rs_ID |
Location |
Functional Annotation |
rs3799976 |
Chr6:44835622(Fwd) |
NMD_transcript_variant; intron_variant |
rs9353524 |
Chr6:88837616(Fwd) |
|
rs12525009 |
Chr6:44875843(Fwd) |
NMD_transcript_variant; intron_variant |
rs806371 |
Chr6:88856363(Fwd) |
intron_variant; upstream_gene_variant |
rs7763421 |
Chr6:44877313(Fwd) |
NMD_transcript_variant; intron_variant |
rs806372 |
Chr6:88856563(Fwd) |
intron_variant; upstream_gene_variant |
rs10948183 |
Chr6:44880881(Fwd) |
NMD_transcript_variant; intron_variant |
rs806374 |
Chr6:88857320(Fwd) |
intron_variant; upstream_gene_variant |
rs12526711 |
Chr6:44883873(Fwd) |
NMD_transcript_variant; intron_variant |
rs806376 |
Chr6:88858648(Fwd) |
5_prime_UTR_variant; intron_variant; upstream_gene_variant |
rs17422760 |
Chr6:44885288(Fwd) |
NMD_transcript_variant; intron_variant |
rs806379 |
Chr6:88861267(Fwd) |
intron_variant; upstream_gene_variant |
rs4711807 |
Chr6:44911652(Fwd) |
NMD_transcript_variant; intron_variant |
rs806375 |
Chr6:88858521(Fwd) |
5_prime_UTR_variant; intron_variant; upstream_gene_variant |
rs7749865 |
Chr6:44918406(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948188 |
Chr6:44926212(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs9472409 |
Chr6:44926431(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs13215618 |
Chr6:44936568(Fwd) |
NMD_transcript_variant; intron_variant |
rs1202198 |
Chr6:20145879(Fwd) |
intron_variant |
rs13216116 |
Chr6:44936681(Fwd) |
NMD_transcript_variant; intron_variant |
rs1212547 |
Chr6:20146507(Fwd) |
intron_variant |
rs10948192 |
Chr6:44947321(Fwd) |
NMD_transcript_variant; intron_variant |
rs520188 |
Chr6:19992265(Fwd) |
|
rs9472416 |
Chr6:44950963(Fwd) |
NMD_transcript_variant; intron_variant |
rs7740484 |
Chr6:137161671(Fwd) |
intron_variant |
rs2457342 |
Chr6:20094030(Fwd) |
|
rs11967188 |
Chr6:44956925(Fwd) |
NMD_transcript_variant; intron_variant |
rs2012700 |
Chr6:137179387(Fwd) |
intron_variant; upstream_gene_variant |
rs2472756 |
Chr6:20120469(Fwd) |
intron_variant |
rs17424547 |
Chr6:44988970(Fwd) |
NMD_transcript_variant; intron_variant |
rs932589 |
Chr6:137083138(Fwd) |
intron_variant |
rs10484637 |
Chr6:20123817(Fwd) |
downstream_gene_variant; intron_variant |
rs1971482 |
Chr6:44991113(Fwd) |
NMD_transcript_variant; intron_variant |
rs6941968 |
Chr6:18780110(Fwd) |
|
rs1022690 |
Chr6:137085296(Fwd) |
intron_variant |
rs2839922 |
Chr6:20134819(Fwd) |
intron_variant |
rs6925467 |
Chr6:44998038(Fwd) |
NMD_transcript_variant; intron_variant |
rs12210137 |
Chr6:18788778(Fwd) |
|
rs9402845 |
Chr6:137089522(Fwd) |
intron_variant |
rs843327 |
Chr6:20145314(Fwd) |
intron_variant |
rs1329714 |
Chr6:45003335(Fwd) |
NMD_transcript_variant; intron_variant |
rs2328312 |
Chr6:18789757(Fwd) |
|
rs9402846 |
Chr6:137093377(Fwd) |
intron_variant |
rs9369529 |
Chr6:45004533(Fwd) |
NMD_transcript_variant; intron_variant |
rs2208856 |
Chr6:18789964(Fwd) |
|
rs9321570 |
Chr6:137095679(Fwd) |
intron_variant |
rs10948198 |
Chr6:45009164(Fwd) |
NMD_transcript_variant; intron_variant |
rs12205846 |
Chr6:18791791(Fwd) |
|
rs11154886 |
Chr6:137099124(Fwd) |
feature_truncation; intron_variant |
rs12529490 |
Chr6:45018251(Fwd) |
NMD_transcript_variant; intron_variant |
rs12211654 |
Chr6:18795083(Fwd) |
|
rs1570054 |
Chr6:137101726(Fwd) |
intron_variant |
rs12205071 |
Chr6:45021215(Fwd) |
NMD_transcript_variant; intron_variant |
rs13193326 |
Chr6:18812605(Fwd) |
|
rs9494569 |
Chr6:137104793(Fwd) |
intron_variant |
rs969211 |
Chr6:45022378(Fwd) |
NMD_transcript_variant; intron_variant |
rs10949550 |
Chr6:18816997(Fwd) |
|
rs9483947 |
Chr6:137105400(Fwd) |
intron_variant |
rs793843 |
Chr6:24217216(Fwd) |
intron_variant |
rs4412189 |
Chr6:45023226(Fwd) |
NMD_transcript_variant; intron_variant |
rs952723 |
Chr6:18819634(Fwd) |
|
rs6912539 |
Chr6:137108757(Fwd) |
intron_variant |
rs9295620 |
Chr6:24255044(Fwd) |
intron_variant |
rs2186062 |
Chr6:45023732(Fwd) |
NMD_transcript_variant; intron_variant |
rs6909029 |
Chr6:18822318(Fwd) |
|
rs4524621 |
Chr6:137111664(Fwd) |
intron_variant |
rs870601 |
Chr6:24261060(Fwd) |
intron_variant |
rs12208023 |
Chr6:45024687(Fwd) |
NMD_transcript_variant; intron_variant |
rs1418966 |
Chr6:18822483(Fwd) |
|
rs3734552 |
Chr6:137112633(Fwd) |
intron_variant |
rs9379649 |
Chr6:24264771(Fwd) |
intron_variant |
rs4707436 |
Chr6:88851751(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs7763450 |
Chr6:45029896(Fwd) |
NMD_transcript_variant; intron_variant |
rs12193218 |
Chr6:18825212(Fwd) |
|
rs3757165 |
Chr6:137116019(Fwd) |
upstream_gene_variant |
rs6456601 |
Chr6:24266739(Fwd) |
intron_variant |
rs9359765 |
Chr6:88826436(Fwd) |
|
rs227849 |
Chr6:44698708(Fwd) |
|
rs6904238 |
Chr6:18831223(Fwd) |
|
rs3903660 |
Chr6:137119578(Fwd) |
|
rs10806986 |
Chr6:24272240(Fwd) |
intron_variant |
rs9397744 |
Chr6:155073206(Fwd) |
intron_variant; nc_transcript_variant |
rs10485171 |
Chr6:88843390(Fwd) |
|
rs9472336 |
Chr6:44710392(Fwd) |
|
rs4142204 |
Chr6:18831438(Fwd) |
|
rs2327760 |
Chr6:137121796(Fwd) |
|
rs12216513 |
Chr6:24273873(Fwd) |
intron_variant |
rs7752180 |
Chr6:155093458(Fwd) |
intron_variant; nc_transcript_variant |
rs7766029 |
Chr6:88847435(Fwd) |
downstream_gene_variant |
rs2798509 |
Chr6:78210763(Fwd) |
downstream_gene_variant |
rs764397 |
Chr6:44710771(Fwd) |
|
rs6928682 |
Chr6:18781294(Fwd) |
|
rs7746446 |
Chr6:137132896(Fwd) |
|
rs12055879 |
Chr6:24274117(Fwd) |
intron_variant |
rs9397747 |
Chr6:155106151(Fwd) |
intron_variant; nc_transcript_variant |
rs1408260 |
Chr6:88821736(Fwd) |
|
rs1539626 |
Chr6:78214023(Fwd) |
|
rs2211393 |
Chr6:44716366(Fwd) |
|
rs7773099 |
Chr6:18797502(Fwd) |
|
rs7746644 |
Chr6:137133118(Fwd) |
|
rs807700 |
Chr6:24274405(Fwd) |
intron_variant |
rs3800005 |
Chr6:155113108(Fwd) |
intron_variant; nc_transcript_variant |
rs1419088 |
Chr6:78214540(Fwd) |
|
rs1338908 |
Chr6:44728812(Fwd) |
|
rs2328313 |
Chr6:18805214(Fwd) |
|
rs9321572 |
Chr6:137134513(Fwd) |
|
rs807722 |
Chr6:24279935(Fwd) |
intron_variant |
rs9371352 |
Chr6:155133680(Fwd) |
intron_variant |
rs1777753 |
Chr6:78216254(Fwd) |
|
rs4714819 |
Chr6:44735285(Fwd) |
|
rs10949547 |
Chr6:18805872(Fwd) |
|
rs9494573 |
Chr6:137135004(Fwd) |
|
rs9379650 |
Chr6:24286952(Fwd) |
intron_variant |
rs3087697 |
Chr6:155133742(Fwd) |
intron_variant |
rs2798956 |
Chr6:78219345(Fwd) |
|
rs10949548 |
Chr6:18806126(Fwd) |
|
rs9494574 |
Chr6:137135077(Fwd) |
|
rs3789228 |
Chr6:24287551(Fwd) |
intron_variant |
rs12201149 |
Chr6:155162163(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2798957 |
Chr6:78219744(Fwd) |
|
rs2038557 |
Chr6:44740471(Fwd) |
|
rs10949549 |
Chr6:18806175(Fwd) |
|
rs10223555 |
Chr6:137136060(Fwd) |
|
rs2274305 |
Chr6:24291203(Fwd) |
missense_variant |
rs9371824 |
Chr6:155029064(Fwd) |
downstream_gene_variant |
rs1777759 |
Chr6:78222394(Fwd) |
|
rs2038556 |
Chr6:44740568(Fwd) |
|
rs1609637 |
Chr6:18807244(Fwd) |
|
rs9321574 |
Chr6:137137826(Fwd) |
|
rs10946689 |
Chr6:24297900(Fwd) |
intron_variant |
rs4870310 |
Chr6:155033087(Fwd) |
downstream_gene_variant |
rs1213380 |
Chr6:78227714(Fwd) |
|
rs9385780 |
Chr6:137307421(Fwd) |
intron_variant; nc_transcript_variant |
rs2040032 |
Chr6:44743009(Fwd) |
|
rs2328316 |
Chr6:18809642(Fwd) |
|
rs1321469 |
Chr6:137139518(Fwd) |
upstream_gene_variant |
rs2328208 |
Chr6:24285571(Fwd) |
intron_variant |
rs6932758 |
Chr6:155049193(Fwd) |
|
rs1213381 |
Chr6:78227749(Fwd) |
|
rs941936 |
Chr6:137320603(Fwd) |
downstream_gene_variant; feature_truncation; nc_transcript_variant; non_coding_exon_variant |
rs9472360 |
Chr6:44747410(Fwd) |
|
rs12205069 |
Chr6:18810974(Fwd) |
|
rs1150637 |
Chr6:16731227(Fwd) |
intron_variant; nc_transcript_variant |
rs1998164 |
Chr6:137140077(Fwd) |
upstream_gene_variant |
rs9467080 |
Chr6:24217261(Fwd) |
intron_variant |
rs3828933 |
Chr6:155053973(Fwd) |
upstream_gene_variant |
rs1343484 |
Chr6:78234365(Fwd) |
|
rs1475119 |
Chr6:137321910(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs1342370 |
Chr6:44747732(Fwd) |
|
rs2328317 |
Chr6:18818868(Fwd) |
|
rs651702 |
Chr6:16744616(Fwd) |
intron_variant; nc_transcript_variant |
rs3757167 |
Chr6:137140993(Fwd) |
upstream_gene_variant |
rs4052671 |
Chr6:24223579(Fwd) |
intron_variant |
rs7744421 |
Chr6:155094764(Fwd) |
intron_variant; nc_transcript_variant |
rs1778248 |
Chr6:78235034(Fwd) |
|
rs4896228 |
Chr6:137327814(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1418434 |
Chr6:44748365(Fwd) |
|
rs1935989 |
Chr6:18821264(Fwd) |
|
rs547491 |
Chr6:16745530(Fwd) |
intron_variant; nc_transcript_variant |
rs3757169 |
Chr6:137142946(Fwd) |
upstream_gene_variant |
rs11757999 |
Chr6:24250820(Fwd) |
intron_variant |
rs3800006 |
Chr6:155099371(Fwd) |
intron_variant; nc_transcript_variant |
rs1778245 |
Chr6:78235457(Fwd) |
|
rs9402865 |
Chr6:137333851(Fwd) |
intron_variant; nc_transcript_variant |
rs4711798 |
Chr6:44750777(Fwd) |
|
rs1418965 |
Chr6:18822462(Fwd) |
|
rs500803 |
Chr6:16754454(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7764028 |
Chr6:137150543(Fwd) |
intron_variant |
rs1109332 |
Chr6:24262457(Fwd) |
intron_variant |
rs4870312 |
Chr6:155120819(Fwd) |
intron_variant |
rs1777783 |
Chr6:78235478(Fwd) |
|
rs1744053 |
Chr6:137308869(Fwd) |
intron_variant; nc_transcript_variant |
rs9472362 |
Chr6:44751285(Fwd) |
|
rs1015211 |
Chr6:18834871(Fwd) |
|
rs2927 |
Chr6:16758112(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs9494579 |
Chr6:137153974(Fwd) |
downstream_gene_variant; intron_variant |
rs11754278 |
Chr6:24279076(Fwd) |
intron_variant |
rs9322480 |
Chr6:155128332(Fwd) |
intron_variant |
rs1777784 |
Chr6:78235972(Fwd) |
|
rs1775326 |
Chr6:137307444(Fwd) |
intron_variant; nc_transcript_variant |
rs1557143 |
Chr6:44756415(Fwd) |
|
rs660586 |
Chr6:16744053(Fwd) |
intron_variant; nc_transcript_variant |
rs6570104 |
Chr6:137154620(Fwd) |
downstream_gene_variant; intron_variant |
rs3789224 |
Chr6:24280101(Fwd) |
intron_variant |
rs12523716 |
Chr6:155145017(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1777785 |
Chr6:78236000(Fwd) |
|
rs1629938 |
Chr6:137307713(Fwd) |
intron_variant; nc_transcript_variant |
rs1293457 |
Chr6:44758098(Fwd) |
|
rs492412 |
Chr6:16744072(Fwd) |
intron_variant; nc_transcript_variant |
rs1321473 |
Chr6:137158764(Fwd) |
intron_variant |
rs17302512 |
Chr6:24281335(Fwd) |
intron_variant |
rs9375 |
Chr6:155155039(Fwd) |
3_prime_UTR_variant; intron_variant; nc_transcript_variant |
rs1674203 |
Chr6:78236614(Fwd) |
|
rs1632514 |
Chr6:137308040(Fwd) |
intron_variant; nc_transcript_variant |
rs4711799 |
Chr6:44765780(Fwd) |
|
rs493352 |
Chr6:16744169(Fwd) |
intron_variant; nc_transcript_variant |
rs6939424 |
Chr6:137160983(Fwd) |
intron_variant |
rs11754080 |
Chr6:24284244(Fwd) |
intron_variant |
rs4292533 |
Chr6:155043595(Fwd) |
|
rs1625213 |
Chr6:78237746(Fwd) |
|
rs1744069 |
Chr6:137309937(Fwd) |
intron_variant; nc_transcript_variant |
rs12190136 |
Chr6:44767072(Fwd) |
|
rs639621 |
Chr6:16744265(Fwd) |
intron_variant; nc_transcript_variant |
rs9402850 |
Chr6:137164622(Fwd) |
intron_variant |
rs17302582 |
Chr6:24285922(Fwd) |
intron_variant |
rs7752542 |
Chr6:155046854(Fwd) |
|
rs1623600 |
Chr6:78237904(Fwd) |
|
rs1293467 |
Chr6:44769204(Fwd) |
|
rs648411 |
Chr6:16744500(Fwd) |
intron_variant; nc_transcript_variant |
rs9399197 |
Chr6:137164798(Fwd) |
intron_variant |
rs3789225 |
Chr6:24286488(Fwd) |
intron_variant |
rs9384238 |
Chr6:155057314(Fwd) |
intron_variant; nc_transcript_variant |
rs1419162 |
Chr6:78241057(Fwd) |
|
rs929614 |
Chr6:44771934(Fwd) |
|
rs717088 |
Chr6:137179449(Fwd) |
intron_variant; upstream_gene_variant |
rs17302729 |
Chr6:24288724(Fwd) |
intron_variant |
rs6911728 |
Chr6:155057907(Fwd) |
intron_variant; nc_transcript_variant |
rs1458440 |
Chr6:78244371(Fwd) |
|
rs6910749 |
Chr6:44773892(Fwd) |
downstream_gene_variant |
rs9373174 |
Chr6:137185164(Fwd) |
intron_variant |
rs2296538 |
Chr6:24289593(Fwd) |
intron_variant |
rs7761794 |
Chr6:155064675(Fwd) |
intron_variant; nc_transcript_variant |
rs10943468 |
Chr6:78246516(Fwd) |
|
rs7754698 |
Chr6:44782717(Fwd) |
NMD_transcript_variant; intron_variant |
rs1474987 |
Chr6:137185293(Fwd) |
intron_variant |
rs3804327 |
Chr6:24292282(Fwd) |
intron_variant |
rs4869833 |
Chr6:155065902(Fwd) |
intron_variant; nc_transcript_variant |
rs2320724 |
Chr6:78247707(Fwd) |
|
rs6904015 |
Chr6:44785502(Fwd) |
NMD_transcript_variant; intron_variant |
rs1884940 |
Chr6:137187641(Fwd) |
intron_variant |
rs1091047 |
Chr6:24295256(Fwd) |
intron_variant |
rs7770922 |
Chr6:155076853(Fwd) |
intron_variant; nc_transcript_variant |
rs2609060 |
Chr6:78251205(Fwd) |
|
rs9395049 |
Chr6:44792718(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs9321578 |
Chr6:137188609(Fwd) |
intron_variant |
rs9322476 |
Chr6:155084269(Fwd) |
intron_variant; nc_transcript_variant |
rs2609063 |
Chr6:78251854(Fwd) |
|
rs9369514 |
Chr6:44797271(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs6936400 |
Chr6:137206262(Fwd) |
intron_variant |
rs9322477 |
Chr6:155084385(Fwd) |
intron_variant; nc_transcript_variant |
rs2609067 |
Chr6:78253681(Fwd) |
|
rs3799967 |
Chr6:44798701(Fwd) |
NMD_transcript_variant; intron_variant |
rs1342645 |
Chr6:137207304(Fwd) |
intron_variant |
rs9371351 |
Chr6:155084927(Fwd) |
intron_variant; nc_transcript_variant |
rs1674212 |
Chr6:78254290(Fwd) |
|
rs3799968 |
Chr6:44805377(Fwd) |
NMD_transcript_variant; intron_variant |
rs11154885 |
Chr6:137099064(Fwd) |
intron_variant |
rs9397202 |
Chr6:155085094(Fwd) |
intron_variant; nc_transcript_variant |
rs1778267 |
Chr6:78254650(Fwd) |
|
rs6910294 |
Chr6:44812565(Fwd) |
NMD_transcript_variant; intron_variant |
rs927182 |
Chr6:137162299(Fwd) |
intron_variant |
rs7744890 |
Chr6:155087842(Fwd) |
intron_variant; nc_transcript_variant |
rs2798975 |
Chr6:78257649(Fwd) |
|
rs3799971 |
Chr6:44819319(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799476 |
Chr6:137184073(Fwd) |
intron_variant |
rs9397745 |
Chr6:155091468(Fwd) |
intron_variant; nc_transcript_variant |
rs2609072 |
Chr6:78258011(Fwd) |
|
rs9395051 |
Chr6:44825715(Fwd) |
NMD_transcript_variant; intron_variant |
rs9494587 |
Chr6:137184492(Fwd) |
intron_variant |
rs9479954 |
Chr6:155092199(Fwd) |
intron_variant; nc_transcript_variant |
rs2798976 |
Chr6:78258171(Fwd) |
|
rs9369516 |
Chr6:44833598(Fwd) |
NMD_transcript_variant; intron_variant |
rs1884939 |
Chr6:137187606(Fwd) |
intron_variant |
rs7762129 |
Chr6:155094988(Fwd) |
intron_variant; nc_transcript_variant |
rs1545665 |
Chr6:78259610(Fwd) |
|
rs7754378 |
Chr6:44863106(Fwd) |
NMD_transcript_variant; intron_variant |
rs2050713 |
Chr6:137194033(Fwd) |
intron_variant |
rs10872710 |
Chr6:155096462(Fwd) |
intron_variant; nc_transcript_variant |
rs9352484 |
Chr6:78197122(Fwd) |
|
rs538801 |
Chr6:44875762(Fwd) |
NMD_transcript_variant; intron_variant |
rs9494591 |
Chr6:137196695(Fwd) |
intron_variant |
rs9479956 |
Chr6:155102802(Fwd) |
intron_variant; nc_transcript_variant |
rs2798950 |
Chr6:78198521(Fwd) |
|
rs6458415 |
Chr6:44881592(Fwd) |
NMD_transcript_variant; intron_variant |
rs7750251 |
Chr6:137203746(Fwd) |
intron_variant |
rs9384241 |
Chr6:155105239(Fwd) |
intron_variant; nc_transcript_variant |
rs9343616 |
Chr6:78198764(Fwd) |
|
rs3799981 |
Chr6:44882380(Fwd) |
NMD_transcript_variant; intron_variant |
rs7750763 |
Chr6:137204016(Fwd) |
intron_variant |
rs9478582 |
Chr6:155105997(Fwd) |
intron_variant; nc_transcript_variant |
rs2798506 |
Chr6:78200726(Fwd) |
|
rs9367211 |
Chr6:44885305(Fwd) |
NMD_transcript_variant; intron_variant |
rs9321580 |
Chr6:137204280(Fwd) |
intron_variant |
rs9478583 |
Chr6:155106052(Fwd) |
intron_variant; nc_transcript_variant |
rs1936158 |
Chr6:78184375(Fwd) |
|
rs3799984 |
Chr6:44893640(Fwd) |
NMD_transcript_variant; intron_variant |
rs1342644 |
Chr6:137206928(Fwd) |
intron_variant |
rs9397749 |
Chr6:155111359(Fwd) |
intron_variant; nc_transcript_variant |
rs1213369 |
Chr6:78178257(Fwd) |
upstream_gene_variant |
rs3778507 |
Chr6:44896803(Fwd) |
NMD_transcript_variant; intron_variant |
rs9321581 |
Chr6:137209311(Fwd) |
intron_variant |
rs6940633 |
Chr6:155115039(Fwd) |
downstream_gene_variant; intron_variant |
rs16889516 |
Chr6:24608559(Fwd) |
intron_variant |
rs1062966 |
Chr6:41652604(Fwd) |
downstream_gene_variant; synonymous_variant; upstream_gene_variant |
rs3799986 |
Chr6:44900253(Fwd) |
NMD_transcript_variant; intron_variant |
rs9321582 |
Chr6:137218692(Fwd) |
downstream_gene_variant; intron_variant |
rs7740797 |
Chr6:155121259(Fwd) |
intron_variant |
rs16889556 |
Chr6:24641605(Fwd) |
intron_variant |
rs9369302 |
Chr6:41664121(Fwd) |
intron_variant; upstream_gene_variant |
rs10948186 |
Chr6:44903248(Fwd) |
NMD_transcript_variant; intron_variant |
rs9494600 |
Chr6:137241328(Fwd) |
upstream_gene_variant |
rs3757291 |
Chr6:155124583(Fwd) |
intron_variant |
rs10456309 |
Chr6:24589562(Fwd) |
intron_variant |
rs2842646 |
Chr6:41646885(Fwd) |
downstream_gene_variant |
rs9472407 |
Chr6:44908800(Fwd) |
NMD_transcript_variant; intron_variant |
rs9494601 |
Chr6:137241350(Fwd) |
upstream_gene_variant |
rs9479959 |
Chr6:155125353(Fwd) |
intron_variant |
rs13209442 |
Chr6:24597176(Fwd) |
intron_variant; upstream_gene_variant |
rs973361 |
Chr6:41647403(Fwd) |
downstream_gene_variant |
rs12190513 |
Chr6:44920679(Fwd) |
NMD_transcript_variant; intron_variant |
rs9389450 |
Chr6:137243020(Fwd) |
upstream_gene_variant |
rs3800002 |
Chr6:155127964(Fwd) |
intron_variant |
rs17307430 |
Chr6:24599574(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs2073157 |
Chr6:41655005(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10948187 |
Chr6:44921320(Fwd) |
NMD_transcript_variant; intron_variant |
rs9478586 |
Chr6:155128944(Fwd) |
intron_variant |
rs12210684 |
Chr6:24601804(Fwd) |
downstream_gene_variant; intron_variant |
rs2073156 |
Chr6:41657328(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1980265 |
Chr6:44928868(Fwd) |
NMD_transcript_variant; intron_variant |
rs6925900 |
Chr6:155134995(Fwd) |
intron_variant |
rs10946707 |
Chr6:24608307(Fwd) |
intron_variant |
rs4472338 |
Chr6:41664727(Fwd) |
intron_variant |
rs1521355 |
Chr6:44932755(Fwd) |
NMD_transcript_variant; intron_variant |
rs7766968 |
Chr6:155136501(Fwd) |
intron_variant |
rs11757448 |
Chr6:24613438(Fwd) |
intron_variant |
rs2246159 |
Chr6:41650975(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs636845 |
Chr6:44935341(Fwd) |
NMD_transcript_variant; intron_variant |
rs2351848 |
Chr6:155137273(Fwd) |
intron_variant |
rs13206235 |
Chr6:24613847(Fwd) |
intron_variant |
rs494982 |
Chr6:44937255(Fwd) |
NMD_transcript_variant; intron_variant |
rs2351845 |
Chr6:155140291(Fwd) |
intron_variant; upstream_gene_variant |
rs12209409 |
Chr6:24616989(Fwd) |
intron_variant |
rs10948190 |
Chr6:44942300(Fwd) |
NMD_transcript_variant; intron_variant |
rs12202939 |
Chr6:155147879(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs11759149 |
Chr6:24628090(Fwd) |
intron_variant |
rs2396369 |
Chr6:44946463(Fwd) |
NMD_transcript_variant; intron_variant |
rs10485354 |
Chr6:155149943(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs12195384 |
Chr6:24638300(Fwd) |
intron_variant |
rs2396371 |
Chr6:44946550(Fwd) |
NMD_transcript_variant; intron_variant |
rs911191 |
Chr6:155152311(Fwd) |
intron_variant; upstream_gene_variant |
rs12207801 |
Chr6:24690449(Fwd) |
intron_variant; nc_transcript_variant |
rs1360197 |
Chr6:44949630(Fwd) |
NMD_transcript_variant; intron_variant |
rs12199781 |
Chr6:155162121(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs6925017 |
Chr6:44950828(Fwd) |
NMD_transcript_variant; intron_variant |
rs4870317 |
Chr6:155196194(Fwd) |
intron_variant; nc_transcript_variant |
rs10948194 |
Chr6:44951990(Fwd) |
NMD_transcript_variant; intron_variant |
rs12528403 |
Chr6:155210588(Fwd) |
intron_variant; nc_transcript_variant |
rs9357464 |
Chr6:44952441(Fwd) |
NMD_transcript_variant; intron_variant |
rs13202898 |
Chr6:155211015(Fwd) |
intron_variant; nc_transcript_variant |
rs976699 |
Chr6:44952852(Fwd) |
NMD_transcript_variant; intron_variant |
rs7753068 |
Chr6:155219158(Fwd) |
intron_variant; nc_transcript_variant |
rs1329716 |
Chr6:44953758(Fwd) |
NMD_transcript_variant; intron_variant |
rs1980602 |
Chr6:155156221(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7775717 |
Chr6:44967761(Fwd) |
NMD_transcript_variant; intron_variant |
rs7760792 |
Chr6:155218117(Fwd) |
intron_variant; nc_transcript_variant |
rs4711809 |
Chr6:44980341(Fwd) |
NMD_transcript_variant; intron_variant |
rs13196046 |
Chr6:155221284(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7742360 |
Chr6:44998692(Fwd) |
NMD_transcript_variant; intron_variant |
rs9373290 |
Chr6:141219999(Fwd) |
|
rs4398713 |
Chr6:45003928(Fwd) |
NMD_transcript_variant; intron_variant |
rs1970349 |
Chr6:141222516(Fwd) |
|
rs1329713 |
Chr6:45004028(Fwd) |
NMD_transcript_variant; intron_variant |
rs9376548 |
Chr6:141262806(Fwd) |
|
rs1023090 |
Chr6:45012381(Fwd) |
NMD_transcript_variant; intron_variant |
rs9385929 |
Chr6:141316206(Fwd) |
|
rs9367214 |
Chr6:45025912(Fwd) |
NMD_transcript_variant; intron_variant |
rs12175481 |
Chr6:141319040(Fwd) |
|
rs609643 |
Chr6:44705303(Fwd) |
|
rs9389846 |
Chr6:141327566(Fwd) |
|
rs9463017 |
Chr6:44710304(Fwd) |
|
rs6931291 |
Chr6:141329638(Fwd) |
|
rs1418435 |
Chr6:44710880(Fwd) |
|
rs9403233 |
Chr6:141341163(Fwd) |
|
rs9463040 |
Chr6:44752286(Fwd) |
|
rs4714873 |
Chr6:45772603(Fwd) |
|
rs1970346 |
Chr6:141342927(Fwd) |
|
rs10944276 |
Chr6:87562096(Fwd) |
|
rs720989 |
Chr6:44765535(Fwd) |
|
rs6921261 |
Chr6:45779530(Fwd) |
|
rs9376562 |
Chr6:141353371(Fwd) |
|
rs720988 |
Chr6:44765660(Fwd) |
|
rs7751001 |
Chr6:87684753(Fwd) |
downstream_gene_variant; intron_variant |
rs9389857 |
Chr6:141372966(Fwd) |
|
rs16872574 |
Chr6:44771041(Fwd) |
|
rs11962946 |
Chr6:87690343(Fwd) |
intron_variant |
rs12173616 |
Chr6:141378032(Fwd) |
|
rs524492 |
Chr6:44796596(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs11963002 |
Chr6:87690518(Fwd) |
intron_variant |
rs12055788 |
Chr6:141380648(Fwd) |
|
rs3799965 |
Chr6:44798617(Fwd) |
NMD_transcript_variant; intron_variant |
rs722763 |
Chr6:87692655(Fwd) |
intron_variant |
rs1402599 |
Chr6:44799657(Fwd) |
NMD_transcript_variant; intron_variant |
rs6914350 |
Chr6:87693076(Fwd) |
intron_variant |
rs542444 |
Chr6:44800015(Fwd) |
NMD_transcript_variant; intron_variant |
rs718166 |
Chr6:87693623(Fwd) |
intron_variant |
rs6914761 |
Chr6:141209394(Fwd) |
|
rs722788 |
Chr6:28483150(Fwd) |
intron_variant; nc_transcript_variant |
rs9472376 |
Chr6:44800247(Fwd) |
NMD_transcript_variant; intron_variant |
rs4707335 |
Chr6:87666120(Fwd) |
intron_variant |
rs1856383 |
Chr6:141214192(Fwd) |
|
rs11757235 |
Chr6:28489279(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3823252 |
Chr6:44810418(Fwd) |
NMD_transcript_variant; intron_variant |
rs11961440 |
Chr6:87667226(Fwd) |
intron_variant |
rs651226 |
Chr6:141182922(Fwd) |
|
rs2282851 |
Chr6:33280309(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12110753 |
Chr6:28529994(Fwd) |
|
rs13206526 |
Chr6:44816181(Fwd) |
NMD_transcript_variant; intron_variant |
rs11966308 |
Chr6:87700820(Fwd) |
intron_variant |
rs1879506 |
Chr6:141196356(Fwd) |
|
rs3106191 |
Chr6:33280505(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7738979 |
Chr6:28557312(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs12529522 |
Chr6:44865520(Fwd) |
NMD_transcript_variant; intron_variant |
rs4707340 |
Chr6:87720685(Fwd) |
intron_variant |
rs2066036 |
Chr6:141197113(Fwd) |
|
rs2239839 |
Chr6:33288075(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs1319076 |
Chr6:28662390(Fwd) |
|
rs12530016 |
Chr6:44866322(Fwd) |
NMD_transcript_variant; intron_variant |
rs6909528 |
Chr6:141203038(Fwd) |
|
rs1059231 |
Chr6:33288271(Fwd) |
downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant |
rs12111360 |
Chr6:28667448(Fwd) |
|
rs1329715 |
Chr6:44909515(Fwd) |
NMD_transcript_variant; intron_variant |
rs2328150 |
Chr6:141210470(Fwd) |
|
rs3130275 |
Chr6:33332137(Fwd) |
downstream_gene_variant |
rs3799987 |
Chr6:44925834(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs6942045 |
Chr6:33351696(Fwd) |
|
rs1360195 |
Chr6:44931331(Fwd) |
NMD_transcript_variant; intron_variant |
rs9394145 |
Chr6:33399778(Fwd) |
intron_variant; missense_variant; nc_transcript_variant |
rs9296450 |
Chr6:44953786(Fwd) |
NMD_transcript_variant; intron_variant |
rs1755047 |
Chr6:33431319(Fwd) |
|
rs35687006 |
Chr6:44956622(Fwd) |
NMD_transcript_variant; intron_variant |
rs2772387 |
Chr6:33451578(Fwd) |
|
rs1159131 |
Chr6:44972209(Fwd) |
NMD_transcript_variant; intron_variant |
rs9380365 |
Chr6:33472317(Fwd) |
|
rs4714834 |
Chr6:44978416(Fwd) |
NMD_transcript_variant; intron_variant |
rs9366824 |
Chr6:33521577(Fwd) |
|
rs12528232 |
Chr6:44982593(Fwd) |
NMD_transcript_variant; synonymous_variant |
rs6914422 |
Chr6:33534880(Fwd) |
|
rs1028944 |
Chr6:44989519(Fwd) |
NMD_transcript_variant; intron_variant |
rs9380355 |
Chr6:33426699(Fwd) |
downstream_gene_variant |
rs13201942 |
Chr6:45003827(Fwd) |
NMD_transcript_variant; intron_variant |
rs3130276 |
Chr6:33336930(Fwd) |
upstream_gene_variant |
rs2894599 |
Chr6:44760860(Fwd) |
|
rs456993 |
Chr6:33358278(Fwd) |
upstream_gene_variant |
rs4714825 |
Chr6:44761546(Fwd) |
|
rs465506 |
Chr6:33359008(Fwd) |
upstream_gene_variant |
rs7769218 |
Chr6:44783457(Fwd) |
NMD_transcript_variant; intron_variant |
rs465474 |
Chr6:33359142(Fwd) |
upstream_gene_variant |
rs2139863 |
Chr6:44796139(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs461964 |
Chr6:33360574(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs16869119 |
Chr6:44814892(Fwd) |
NMD_transcript_variant; intron_variant |
rs442745 |
Chr6:33382241(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3799972 |
Chr6:44823273(Fwd) |
NMD_transcript_variant; intron_variant |
rs2772373 |
Chr6:33429672(Fwd) |
downstream_gene_variant |
rs3799974 |
Chr6:44824948(Fwd) |
NMD_transcript_variant; intron_variant |
rs6919161 |
Chr6:44888117(Fwd) |
NMD_transcript_variant; intron_variant |
rs10946675 |
Chr6:24141920(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4512220 |
Chr6:44923138(Fwd) |
5_prime_UTR_variant; NMD_transcript_variant; intron_variant |
rs3181244 |
Chr6:24651388(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1053047 |
Chr6:24147483(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs9472414 |
Chr6:44946506(Fwd) |
NMD_transcript_variant; intron_variant |
rs12524925 |
Chr6:141187255(Fwd) |
|
rs7768291 |
Chr6:24656571(Fwd) |
intron_variant; nc_transcript_variant |
rs3857540 |
Chr6:24158542(Fwd) |
downstream_gene_variant |
rs1023091 |
Chr6:44975022(Fwd) |
NMD_transcript_variant; intron_variant |
rs6917444 |
Chr6:141194073(Fwd) |
|
rs3756819 |
Chr6:24665340(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12211300 |
Chr6:24161869(Fwd) |
upstream_gene_variant |
rs13209827 |
Chr6:44998632(Fwd) |
NMD_transcript_variant; intron_variant |
rs582203 |
Chr6:141133003(Fwd) |
|
rs3777665 |
Chr6:24693523(Fwd) |
intron_variant; nc_transcript_variant |
rs4582376 |
Chr6:24167807(Fwd) |
downstream_gene_variant |
rs13205113 |
Chr6:45003990(Fwd) |
NMD_transcript_variant; intron_variant |
rs647875 |
Chr6:141137751(Fwd) |
|
rs12528762 |
Chr6:45004185(Fwd) |
NMD_transcript_variant; intron_variant |
rs849294 |
Chr6:141185228(Fwd) |
|
rs13211006 |
Chr6:45023076(Fwd) |
NMD_transcript_variant; intron_variant |
rs1521150 |
Chr6:141188713(Fwd) |
|
rs7745506 |
Chr6:45030010(Fwd) |
NMD_transcript_variant; intron_variant |
rs13194620 |
Chr6:141189279(Fwd) |
|
rs12215263 |
Chr6:44831364(Fwd) |
NMD_transcript_variant; intron_variant |
rs12204980 |
Chr6:141217085(Fwd) |
|
rs10948176 |
Chr6:44833913(Fwd) |
NMD_transcript_variant; intron_variant |
rs623571 |
Chr6:141149103(Fwd) |
|
rs9367210 |
Chr6:44863395(Fwd) |
NMD_transcript_variant; intron_variant |
rs681758 |
Chr6:141151806(Fwd) |
|
rs6924185 |
Chr6:45017228(Fwd) |
NMD_transcript_variant; intron_variant |
rs672301 |
Chr6:141153358(Fwd) |
|
rs647781 |
Chr6:141156833(Fwd) |
|
rs643558 |
Chr6:141158127(Fwd) |
|
rs13192352 |
Chr6:78168373(Fwd) |
downstream_gene_variant |
rs644443 |
Chr6:141158321(Fwd) |
|
rs12662392 |
Chr6:78189648(Fwd) |
|
rs584727 |
Chr6:141158509(Fwd) |
|
rs6916063 |
Chr6:78203963(Fwd) |
upstream_gene_variant |
rs609656 |
Chr6:141158557(Fwd) |
|
rs4142329 |
Chr6:78205324(Fwd) |
upstream_gene_variant |
rs637822 |
Chr6:141160325(Fwd) |
|
rs17217509 |
Chr6:18508557(Fwd) |
|
rs1213355 |
Chr6:78205970(Fwd) |
nc_transcript_variant; non_coding_exon_variant |
rs650907 |
Chr6:141160933(Fwd) |
|
rs2876486 |
Chr6:18565176(Fwd) |
|
rs1778259 |
Chr6:78207233(Fwd) |
downstream_gene_variant |
rs627812 |
Chr6:141161200(Fwd) |
|
rs17643023 |
Chr6:18614689(Fwd) |
|
rs4708347 |
Chr6:78223114(Fwd) |
|
rs665541 |
Chr6:141161887(Fwd) |
|
rs6904170 |
Chr6:18668726(Fwd) |
|
rs10943465 |
Chr6:78236296(Fwd) |
|
rs618795 |
Chr6:141164935(Fwd) |
downstream_gene_variant |
rs540362 |
Chr6:18480400(Fwd) |
|
rs1419082 |
Chr6:78236368(Fwd) |
|
rs620151 |
Chr6:141165191(Fwd) |
downstream_gene_variant |
rs12194659 |
Chr6:18487307(Fwd) |
|
rs1458443 |
Chr6:78238672(Fwd) |
|
rs687879 |
Chr6:141165413(Fwd) |
downstream_gene_variant |
rs16880809 |
Chr6:18487773(Fwd) |
|
rs7740769 |
Chr6:18497253(Fwd) |
|
rs564174 |
Chr6:13375911(Fwd) |
intron_variant |
rs1458449 |
Chr6:78251686(Fwd) |
|
rs630983 |
Chr6:141165676(Fwd) |
downstream_gene_variant |
rs12211966 |
Chr6:18488785(Fwd) |
|
rs3798683 |
Chr6:154418414(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12191192 |
Chr6:18540044(Fwd) |
|
rs2798960 |
Chr6:78223228(Fwd) |
|
rs594761 |
Chr6:141166412(Fwd) |
downstream_gene_variant |
rs7775993 |
Chr6:18491731(Fwd) |
|
rs1228814 |
Chr6:78173820(Fwd) |
upstream_gene_variant |
rs12527423 |
Chr6:154312386(Fwd) |
|
rs12215669 |
Chr6:18561460(Fwd) |
|
rs2496162 |
Chr6:13361088(Fwd) |
3_prime_UTR_variant |
rs9352485 |
Chr6:78201542(Fwd) |
upstream_gene_variant |
rs644638 |
Chr6:141166427(Fwd) |
downstream_gene_variant |
rs12202692 |
Chr6:18501753(Fwd) |
|
rs17273700 |
Chr6:78173980(Fwd) |
upstream_gene_variant |
rs17084850 |
Chr6:154314459(Fwd) |
|
rs9477786 |
Chr6:18578438(Fwd) |
|
rs2496161 |
Chr6:13361765(Fwd) |
3_prime_UTR_variant |
rs1343488 |
Chr6:78202442(Fwd) |
upstream_gene_variant |
rs664281 |
Chr6:141168192(Fwd) |
intron_variant; nc_transcript_variant |
rs12203070 |
Chr6:18502447(Fwd) |
|
rs9361235 |
Chr6:78175842(Fwd) |
upstream_gene_variant |
rs969436 |
Chr6:154316413(Fwd) |
|
rs9477787 |
Chr6:18578739(Fwd) |
|
rs2496160 |
Chr6:13361927(Fwd) |
3_prime_UTR_variant |
rs12211608 |
Chr6:78218505(Fwd) |
|
rs596721 |
Chr6:141170616(Fwd) |
intron_variant; nc_transcript_variant |
rs10456833 |
Chr6:18518941(Fwd) |
|
rs1213366 |
Chr6:78176870(Fwd) |
upstream_gene_variant |
rs7738859 |
Chr6:154317754(Fwd) |
|
rs2064173 |
Chr6:18580921(Fwd) |
|
rs9367440 |
Chr6:13365913(Fwd) |
intron_variant |
rs1778258 |
Chr6:78174209(Fwd) |
upstream_gene_variant |
rs672906 |
Chr6:141170923(Fwd) |
intron_variant; nc_transcript_variant |
rs16880897 |
Chr6:18534424(Fwd) |
|
rs1213373 |
Chr6:78182930(Fwd) |
|
rs2050940 |
Chr6:154318091(Fwd) |
|
rs2064174 |
Chr6:18580934(Fwd) |
|
rs510932 |
Chr6:13367516(Fwd) |
intron_variant |
rs12173930 |
Chr6:78186434(Fwd) |
|
rs687815 |
Chr6:141171923(Fwd) |
intron_variant; nc_transcript_variant |
rs6926275 |
Chr6:18559644(Fwd) |
|
rs9361233 |
Chr6:78170062(Fwd) |
downstream_gene_variant |
rs6930430 |
Chr6:154319162(Fwd) |
|
rs2064175 |
Chr6:18581172(Fwd) |
|
rs821277 |
Chr6:13369480(Fwd) |
intron_variant |
rs9359274 |
Chr6:78199922(Fwd) |
|
rs677319 |
Chr6:141175369(Fwd) |
upstream_gene_variant |
rs16880957 |
Chr6:18577253(Fwd) |
|
rs1213357 |
Chr6:78204277(Fwd) |
upstream_gene_variant |
rs6930641 |
Chr6:154319323(Fwd) |
|
rs2179307 |
Chr6:18584198(Fwd) |
|
rs579028 |
Chr6:13369921(Fwd) |
intron_variant |
rs7748725 |
Chr6:78203382(Fwd) |
upstream_gene_variant |
rs806381 |
Chr6:88865901(Fwd) |
intron_variant |
rs626931 |
Chr6:141178958(Fwd) |
upstream_gene_variant |
rs10484370 |
Chr6:18578387(Fwd) |
|
rs1213356 |
Chr6:78204530(Fwd) |
upstream_gene_variant |
rs1116706 |
Chr6:154319434(Fwd) |
|
rs1028335 |
Chr6:18584724(Fwd) |
|
rs492433 |
Chr6:13370705(Fwd) |
intron_variant |
rs2874277 |
Chr6:78221848(Fwd) |
|
rs6454673 |
Chr6:88871049(Fwd) |
intron_variant |
rs12207530 |
Chr6:18592709(Fwd) |
|
rs1361847 |
Chr6:78204639(Fwd) |
upstream_gene_variant |
rs17084868 |
Chr6:154321934(Fwd) |
|
rs11243295 |
Chr6:9026671(Fwd) |
|
rs760828 |
Chr6:18585612(Fwd) |
|
rs4711978 |
Chr6:13370779(Fwd) |
intron_variant |
rs12524589 |
Chr6:78227892(Fwd) |
|
rs10948096 |
Chr6:43784803(Fwd) |
|
rs12193629 |
Chr6:18599110(Fwd) |
|
rs1458416 |
Chr6:78327600(Fwd) |
|
rs17084870 |
Chr6:154322578(Fwd) |
|
rs429460 |
Chr6:9026525(Fwd) |
|
rs10949531 |
Chr6:18588806(Fwd) |
|
rs573109 |
Chr6:13373409(Fwd) |
intron_variant |
rs12213990 |
Chr6:78236854(Fwd) |
|
rs4714698 |
Chr6:43788679(Fwd) |
|
rs12207017 |
Chr6:18599739(Fwd) |
|
rs9383689 |
Chr6:154329853(Fwd) |
upstream_gene_variant |
rs433603 |
Chr6:9025535(Fwd) |
|
rs926378 |
Chr6:18595510(Fwd) |
|
rs517803 |
Chr6:13373569(Fwd) |
intron_variant |
rs13213192 |
Chr6:78254436(Fwd) |
|
rs6911440 |
Chr6:43790250(Fwd) |
|
rs12205683 |
Chr6:18600856(Fwd) |
|
rs1213352 |
Chr6:78191811(Fwd) |
|
rs9285541 |
Chr6:154330629(Fwd) |
upstream_gene_variant |
rs84647 |
Chr6:9027803(Fwd) |
|
rs7770329 |
Chr6:18596034(Fwd) |
|
rs570315 |
Chr6:13378677(Fwd) |
intron_variant |
rs10455332 |
Chr6:78256922(Fwd) |
|
rs6911896 |
Chr6:43790318(Fwd) |
|
rs2050014 |
Chr6:18635980(Fwd) |
|
rs1778255 |
Chr6:78198081(Fwd) |
|
rs1294092 |
Chr6:154335673(Fwd) |
intron_variant |
rs380915 |
Chr6:9031654(Fwd) |
|
rs16880993 |
Chr6:18601324(Fwd) |
|
rs489396 |
Chr6:13379615(Fwd) |
intron_variant |
rs12206859 |
Chr6:78263738(Fwd) |
|
rs6902871 |
Chr6:43791897(Fwd) |
|
rs17700261 |
Chr6:18638471(Fwd) |
|
rs1294091 |
Chr6:154336426(Fwd) |
intron_variant |
rs382323 |
Chr6:9032138(Fwd) |
|
rs575709 |
Chr6:13379725(Fwd) |
intron_variant |
rs1343492 |
Chr6:78268916(Fwd) |
|
rs2396087 |
Chr6:43796058(Fwd) |
|
rs17700526 |
Chr6:18647936(Fwd) |
|
rs7757649 |
Chr6:154336687(Fwd) |
intron_variant |
rs421424 |
Chr6:9022100(Fwd) |
|
rs491278 |
Chr6:13379826(Fwd) |
intron_variant |
rs9361238 |
Chr6:78192215(Fwd) |
|
rs4273687 |
Chr6:43796146(Fwd) |
|
rs9477810 |
Chr6:18656937(Fwd) |
|
rs1294087 |
Chr6:154337595(Fwd) |
intron_variant |
rs548119 |
Chr6:13380418(Fwd) |
intron_variant |
rs12203487 |
Chr6:78158883(Fwd) |
|
rs12660375 |
Chr6:43801582(Fwd) |
|
rs16881045 |
Chr6:18668258(Fwd) |
|
rs1294086 |
Chr6:154337784(Fwd) |
intron_variant |
rs516003 |
Chr6:13381641(Fwd) |
intron_variant |
rs10943458 |
Chr6:78161588(Fwd) |
|
rs6940798 |
Chr6:43793391(Fwd) |
|
rs6927583 |
Chr6:18424430(Fwd) |
intron_variant |
rs712244 |
Chr6:154335150(Fwd) |
intron_variant |
rs2496173 |
Chr6:13382290(Fwd) |
intron_variant |
rs943072 |
Chr6:43795968(Fwd) |
|
rs6924327 |
Chr6:18426143(Fwd) |
intron_variant |
rs476904 |
Chr6:13383430(Fwd) |
intron_variant |
rs2894536 |
Chr6:43801878(Fwd) |
|
rs12191033 |
Chr6:18427127(Fwd) |
intron_variant |
rs501987 |
Chr6:13383830(Fwd) |
intron_variant |
rs6458352 |
Chr6:43792541(Fwd) |
|
rs1886353 |
Chr6:18454163(Fwd) |
intron_variant |
rs531256 |
Chr6:13384746(Fwd) |
intron_variant |
rs6907615 |
Chr6:18694823(Fwd) |
|
rs7760579 |
Chr6:13385108(Fwd) |
intron_variant |
rs9357708 |
Chr6:13385822(Fwd) |
intron_variant |
rs12153966 |
Chr6:13386748(Fwd) |
intron_variant |
rs2184906 |
Chr6:114707360(Fwd) |
intron_variant; nc_transcript_variant |
rs7770078 |
Chr6:13386972(Fwd) |
intron_variant |
rs10484274 |
Chr6:114612973(Fwd) |
intron_variant; nc_transcript_variant |
rs524118 |
Chr6:13387309(Fwd) |
intron_variant |
rs10484273 |
Chr6:114618234(Fwd) |
intron_variant; nc_transcript_variant |
rs2439536 |
Chr6:13387350(Fwd) |
intron_variant |
rs7770227 |
Chr6:114622214(Fwd) |
intron_variant; nc_transcript_variant |
rs10807431 |
Chr6:13387509(Fwd) |
intron_variant |
rs7742475 |
Chr6:114624006(Fwd) |
intron_variant; nc_transcript_variant |
rs7739768 |
Chr6:114626642(Fwd) |
intron_variant; nc_transcript_variant |
rs6927808 |
Chr6:114631425(Fwd) |
intron_variant; nc_transcript_variant |
rs9488369 |
Chr6:114632392(Fwd) |
intron_variant; nc_transcript_variant |
rs785132 |
Chr6:114634471(Fwd) |
intron_variant; nc_transcript_variant |
rs10447428 |
Chr6:114634998(Fwd) |
intron_variant; nc_transcript_variant |
rs10447429 |
Chr6:114635085(Fwd) |
intron_variant; nc_transcript_variant |
rs12216474 |
Chr6:114649839(Fwd) |
intron_variant; nc_transcript_variant |
rs785145 |
Chr6:114650655(Fwd) |
intron_variant; nc_transcript_variant |
rs7349953 |
Chr6:114651277(Fwd) |
intron_variant; nc_transcript_variant |
rs1323056 |
Chr6:114653522(Fwd) |
intron_variant; nc_transcript_variant |
rs1337332 |
Chr6:114696790(Fwd) |
intron_variant; nc_transcript_variant |
rs7738812 |
Chr6:88916603(Fwd) |
|
rs785137 |
Chr6:114655699(Fwd) |
intron_variant; nc_transcript_variant |
rs7754491 |
Chr6:88919215(Fwd) |
|
rs1548225 |
Chr6:114679177(Fwd) |
intron_variant; nc_transcript_variant |
rs7769918 |
Chr6:88920372(Fwd) |
|
rs7763992 |
Chr6:114685980(Fwd) |
intron_variant; nc_transcript_variant |
rs16880396 |
Chr6:88928929(Fwd) |
|
rs2817200 |
Chr6:24584366(Fwd) |
intron_variant |
rs9384900 |
Chr6:114711095(Fwd) |
intron_variant; nc_transcript_variant |
rs7756920 |
Chr6:88930327(Fwd) |
|
rs13218075 |
Chr6:24599246(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs1033394 |
Chr6:114713323(Fwd) |
intron_variant; nc_transcript_variant |
rs7757556 |
Chr6:88930614(Fwd) |
|
rs13204166 |
Chr6:24608687(Fwd) |
intron_variant |
rs760608 |
Chr6:114719447(Fwd) |
intron_variant; nc_transcript_variant |
rs6927294 |
Chr6:88931764(Fwd) |
|
rs7751357 |
Chr6:24625398(Fwd) |
intron_variant |
rs9400717 |
Chr6:114721697(Fwd) |
intron_variant; nc_transcript_variant |
rs6906154 |
Chr6:88940323(Fwd) |
|
rs2179515 |
Chr6:24628203(Fwd) |
intron_variant |
rs9366573 |
Chr6:24628472(Fwd) |
intron_variant |
rs6938069 |
Chr6:24628993(Fwd) |
intron_variant |
rs6917660 |
Chr6:24629106(Fwd) |
intron_variant |
rs9393570 |
Chr6:24629772(Fwd) |
intron_variant |
rs9393571 |
Chr6:24629821(Fwd) |
intron_variant |
rs9358777 |
Chr6:24629839(Fwd) |
intron_variant |
rs6456622 |
Chr6:24631558(Fwd) |
intron_variant |
rs6903205 |
Chr6:24631797(Fwd) |
intron_variant |
rs6923652 |
Chr6:24631960(Fwd) |
intron_variant |
rs6923867 |
Chr6:24632137(Fwd) |
intron_variant |
rs761101 |
Chr6:24632532(Fwd) |
intron_variant |
rs4712835 |
Chr6:24634379(Fwd) |
intron_variant |
rs9358783 |
Chr6:24636270(Fwd) |
intron_variant |
rs2223590 |
Chr6:24637087(Fwd) |
intron_variant |
rs7755563 |
Chr6:24638711(Fwd) |
intron_variant |
rs6456624 |
Chr6:24639223(Fwd) |
intron_variant |
rs7760198 |
Chr6:24639517(Fwd) |
intron_variant |
rs9356940 |
Chr6:24640196(Fwd) |
intron_variant |
rs10806098 |
Chr6:78176009(Fwd) |
upstream_gene_variant |
rs9356941 |
Chr6:24640442(Fwd) |
intron_variant |
rs1303712 |
Chr6:78228544(Fwd) |
|
rs9366575 |
Chr6:24640488(Fwd) |
intron_variant |
rs9379678 |
Chr6:24640615(Fwd) |
intron_variant |
rs2328846 |
Chr6:24645195(Fwd) |
intron_variant |
rs2038135 |
Chr6:24645967(Fwd) |
5_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant |
rs1555090 |
Chr6:24648107(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs761100 |
Chr6:24632642(Fwd) |
intron_variant |
rs9368395 |
Chr6:22033121(Fwd) |
|
rs6917244 |
Chr6:24638047(Fwd) |
intron_variant |
rs10946495 |
Chr6:21999300(Fwd) |
|
rs9358483 |
Chr6:22029621(Fwd) |
|
rs10498704 |
Chr6:22018994(Fwd) |
|
rs3799979 |
Chr6:44845514(Fwd) |
NMD_transcript_variant; intron_variant |
rs4714828 |
Chr6:44846008(Fwd) |
NMD_transcript_variant; intron_variant |
rs10484627 |
Chr6:44884267(Fwd) |
NMD_transcript_variant; intron_variant |
rs608941 |
Chr6:44888740(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948185 |
Chr6:44901727(Fwd) |
NMD_transcript_variant; intron_variant |
rs12196818 |
Chr6:44911414(Fwd) |
NMD_transcript_variant; intron_variant |
rs12214778 |
Chr6:44924412(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs4714830 |
Chr6:44955528(Fwd) |
NMD_transcript_variant; intron_variant |
rs2396372 |
Chr6:44966867(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948197 |
Chr6:44967490(Fwd) |
NMD_transcript_variant; intron_variant |
rs1329710 |
Chr6:44969125(Fwd) |
NMD_transcript_variant; intron_variant |
rs1041332 |
Chr6:45012811(Fwd) |
NMD_transcript_variant; intron_variant |
rs4714836 |
Chr6:45019777(Fwd) |
NMD_transcript_variant; intron_variant |
rs9353525 |
Chr6:88843377(Fwd) |
|
rs3799973 |
Chr6:44823727(Fwd) |
NMD_transcript_variant; intron_variant |
rs806370 |
Chr6:88856331(Fwd) |
intron_variant; upstream_gene_variant |