rs_ID |
Location |
Functional Annotation |
rs1405495 |
Chr12:79799306(Fwd) |
intron_variant; nc_transcript_variant |
rs11111782 |
Chr12:104188476(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1526955 |
Chr12:79800028(Fwd) |
intron_variant; nc_transcript_variant |
rs11055594 |
Chr12:13857437(Fwd) |
intron_variant |
rs11111783 |
Chr12:104188523(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs17005561 |
Chr12:79800344(Fwd) |
intron_variant; nc_transcript_variant |
rs11055595 |
Chr12:13857554(Fwd) |
intron_variant |
rs4964814 |
Chr12:104189384(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs12423434 |
Chr12:79801525(Fwd) |
intron_variant; nc_transcript_variant |
rs12809496 |
Chr12:13857909(Fwd) |
intron_variant |
rs4964806 |
Chr12:104192760(Fwd) |
intron_variant; nc_transcript_variant |
rs4609662 |
Chr12:79802176(Fwd) |
intron_variant; nc_transcript_variant |
rs10492134 |
Chr12:13858882(Fwd) |
intron_variant |
rs4964794 |
Chr12:104194418(Fwd) |
intron_variant; nc_transcript_variant |
rs1358243 |
Chr12:79803909(Fwd) |
intron_variant; nc_transcript_variant |
rs10845827 |
Chr12:13859064(Fwd) |
intron_variant |
rs7134701 |
Chr12:104202691(Fwd) |
intron_variant |
rs1405497 |
Chr12:79804808(Fwd) |
intron_variant; nc_transcript_variant |
rs2300249 |
Chr12:13860067(Fwd) |
intron_variant |
rs11111779 |
Chr12:104185496(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs7295888 |
Chr12:79807346(Fwd) |
intron_variant; nc_transcript_variant |
rs2300250 |
Chr12:13860621(Fwd) |
intron_variant |
rs4964812 |
Chr12:104189615(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs17005588 |
Chr12:79809256(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11055601 |
Chr12:13869312(Fwd) |
intron_variant |
rs10861104 |
Chr12:104189923(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs11612225 |
Chr12:79810422(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4764028 |
Chr12:13855778(Fwd) |
intron_variant |
rs10861105 |
Chr12:104189999(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs17041667 |
Chr12:79811286(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11836523 |
Chr12:13857884(Fwd) |
intron_variant |
rs12228207 |
Chr12:104196734(Fwd) |
intron_variant; upstream_gene_variant |
rs7308297 |
Chr12:79777844(Fwd) |
intron_variant; nc_transcript_variant |
rs2284410 |
Chr12:13859811(Fwd) |
intron_variant |
rs4964289 |
Chr12:104204191(Fwd) |
intron_variant |
rs2400395 |
Chr12:79778358(Fwd) |
intron_variant; nc_transcript_variant |
rs2900314 |
Chr12:13865421(Fwd) |
intron_variant |
rs12229276 |
Chr12:104204771(Fwd) |
intron_variant |
rs7966962 |
Chr12:79779417(Fwd) |
intron_variant; nc_transcript_variant |
rs11111795 |
Chr12:104204830(Fwd) |
intron_variant |
rs11114088 |
Chr12:79794919(Fwd) |
intron_variant; nc_transcript_variant |
rs11111796 |
Chr12:104205928(Fwd) |
intron_variant |
rs1386498 |
Chr12:72398143(Fwd) |
intron_variant |
rs4964780 |
Chr12:104206859(Fwd) |
intron_variant |
rs11179039 |
Chr12:72402186(Fwd) |
intron_variant |
rs3935416 |
Chr12:104206955(Fwd) |
intron_variant |
rs3903502 |
Chr12:72406532(Fwd) |
intron_variant |
rs10861094 |
Chr12:104159716(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10879351 |
Chr12:72406833(Fwd) |
intron_variant |
rs3812803 |
Chr12:104200460(Fwd) |
intron_variant; upstream_gene_variant |
rs9325202 |
Chr12:72407477(Fwd) |
intron_variant |
rs4964786 |
Chr12:104204583(Fwd) |
intron_variant |
rs12322900 |
Chr12:72353257(Fwd) |
NMD_transcript_variant; intron_variant |
rs11111773 |
Chr12:104183848(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs7967686 |
Chr12:72390025(Fwd) |
intron_variant |
rs934845 |
Chr12:104185257(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs10748190 |
Chr12:72406036(Fwd) |
intron_variant |
rs1866296 |
Chr12:104187092(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1352251 |
Chr12:72397894(Fwd) |
intron_variant |
rs12424737 |
Chr12:104196221(Fwd) |
intron_variant; upstream_gene_variant |
rs11179049 |
Chr12:72410021(Fwd) |
intron_variant |
rs11179050 |
Chr12:72410079(Fwd) |
intron_variant |
rs2200579 |
Chr12:72410745(Fwd) |
intron_variant |
rs1386487 |
Chr12:72411212(Fwd) |
feature_truncation; intron_variant |
rs1386486 |
Chr12:72412220(Fwd) |
intron_variant |
rs1386485 |
Chr12:72412367(Fwd) |
intron_variant |
rs1386483 |
Chr12:72412494(Fwd) |
intron_variant |
rs7961819 |
Chr12:13698642(Fwd) |
intron_variant; nc_transcript_variant |
rs1386482 |
Chr12:72412572(Fwd) |
intron_variant |
rs1805247 |
Chr12:13715975(Fwd) |
synonymous_variant |
rs11179052 |
Chr12:72412701(Fwd) |
intron_variant |
rs1806198 |
Chr12:13735144(Fwd) |
intron_variant |
rs10879355 |
Chr12:72413009(Fwd) |
intron_variant |
rs1806199 |
Chr12:13735154(Fwd) |
intron_variant |
rs4469933 |
Chr12:72414717(Fwd) |
intron_variant |
rs1805471 |
Chr12:13736797(Fwd) |
downstream_gene_variant; intron_variant |
rs4430554 |
Chr12:72414858(Fwd) |
intron_variant |
rs7970177 |
Chr12:13738988(Fwd) |
downstream_gene_variant; intron_variant |
rs4488237 |
Chr12:72415034(Fwd) |
intron_variant |
rs1805474 |
Chr12:13742150(Fwd) |
intron_variant; upstream_gene_variant |
rs11179059 |
Chr12:72415206(Fwd) |
intron_variant |
rs888150 |
Chr12:13745044(Fwd) |
intron_variant; upstream_gene_variant |
rs4474484 |
Chr12:72415446(Fwd) |
intron_variant |
rs10772695 |
Chr12:13745348(Fwd) |
intron_variant; upstream_gene_variant |
rs4290270 |
Chr12:72416235(Fwd) |
synonymous_variant |
rs1805510 |
Chr12:13751252(Fwd) |
intron_variant |
rs1805522 |
Chr12:13761741(Fwd) |
synonymous_variant |
rs1805483 |
Chr12:13765238(Fwd) |
intron_variant |
rs1805544 |
Chr12:13787834(Fwd) |
intron_variant |
rs2216217 |
Chr12:13790009(Fwd) |
intron_variant |
rs1805546 |
Chr12:13791508(Fwd) |
intron_variant |
rs2268101 |
Chr12:13802317(Fwd) |
intron_variant |
rs2284403 |
Chr12:13804150(Fwd) |
intron_variant |
rs2284405 |
Chr12:13804560(Fwd) |
intron_variant |
rs2300237 |
Chr12:13813270(Fwd) |
intron_variant |
rs1805519 |
Chr12:13753852(Fwd) |
intron_variant |
rs1805476 |
Chr12:13714363(Fwd) |
3_prime_UTR_variant |
rs1805481 |
Chr12:13763455(Fwd) |
intron_variant |
rs2270359 |
Chr12:13722313(Fwd) |
intron_variant |
rs1805485 |
Chr12:13766887(Fwd) |
intron_variant |
rs10772694 |
Chr12:13739350(Fwd) |
downstream_gene_variant; intron_variant |
rs1805539 |
Chr12:13770190(Fwd) |
intron_variant |
rs10845814 |
Chr12:13772993(Fwd) |
intron_variant |
rs2284402 |
Chr12:13775958(Fwd) |
intron_variant |
rs432794 |
Chr12:63070497(Fwd) |
intron_variant; nc_transcript_variant |
rs4764023 |
Chr12:13794318(Fwd) |
intron_variant |
rs11174611 |
Chr12:63098521(Fwd) |
intron_variant; nc_transcript_variant |
rs10845819 |
Chr12:13805633(Fwd) |
intron_variant |
rs4763192 |
Chr12:63106708(Fwd) |
intron_variant; nc_transcript_variant |
rs2300234 |
Chr12:13803051(Fwd) |
intron_variant |
rs4763196 |
Chr12:63163070(Fwd) |
intron_variant; nc_transcript_variant |
rs7978482 |
Chr12:72365973(Fwd) |
intron_variant |
rs2300235 |
Chr12:13810845(Fwd) |
intron_variant |
rs17732506 |
Chr12:63041307(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant |
rs1843810 |
Chr12:72367420(Fwd) |
intron_variant |
rs2300236 |
Chr12:13811372(Fwd) |
intron_variant |
rs17676109 |
Chr12:63050251(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7300641 |
Chr12:72368571(Fwd) |
intron_variant |
rs2300238 |
Chr12:13813330(Fwd) |
intron_variant |
rs11179003 |
Chr12:72343287(Fwd) |
NMD_transcript_variant; intron_variant |
rs1805473 |
Chr12:13739553(Fwd) |
downstream_gene_variant; intron_variant |
rs17099949 |
Chr12:64336805(Fwd) |
intron_variant; nc_transcript_variant |
rs11179004 |
Chr12:72344430(Fwd) |
NMD_transcript_variant; intron_variant |
rs980365 |
Chr12:13820027(Fwd) |
intron_variant |
rs17711166 |
Chr12:64447812(Fwd) |
intron_variant; nc_transcript_variant |
rs10879344 |
Chr12:72344561(Fwd) |
NMD_transcript_variant; intron_variant |
rs2268102 |
Chr12:13822239(Fwd) |
intron_variant |
rs699629 |
Chr12:64521141(Fwd) |
intron_variant; upstream_gene_variant |
rs11179015 |
Chr12:72360777(Fwd) |
downstream_gene_variant; intron_variant |
rs1008619 |
Chr12:13826407(Fwd) |
intron_variant |
rs789738 |
Chr12:64536009(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11179017 |
Chr12:72361408(Fwd) |
downstream_gene_variant; intron_variant |
rs7313149 |
Chr12:13828287(Fwd) |
intron_variant |
rs12227635 |
Chr12:64358475(Fwd) |
intron_variant; nc_transcript_variant |
rs11179018 |
Chr12:72361431(Fwd) |
downstream_gene_variant; intron_variant |
rs10772698 |
Chr12:13829541(Fwd) |
intron_variant |
rs11179000 |
Chr12:72338628(Fwd) |
NMD_transcript_variant; intron_variant |
rs11179022 |
Chr12:72370746(Fwd) |
intron_variant |
rs2193150 |
Chr12:13831339(Fwd) |
intron_variant |
rs10748185 |
Chr12:72335855(Fwd) |
NMD_transcript_variant; intron_variant |
rs12231408 |
Chr12:72373904(Fwd) |
intron_variant |
rs7970144 |
Chr12:13832945(Fwd) |
intron_variant; upstream_gene_variant |
rs10748186 |
Chr12:72335988(Fwd) |
NMD_transcript_variant; intron_variant |
rs11179032 |
Chr12:72382466(Fwd) |
intron_variant |
rs4764025 |
Chr12:13834761(Fwd) |
intron_variant; upstream_gene_variant |
rs11830353 |
Chr12:72347983(Fwd) |
NMD_transcript_variant; intron_variant |
rs10492133 |
Chr12:13834813(Fwd) |
intron_variant; upstream_gene_variant |
rs10744037 |
Chr12:13835404(Fwd) |
intron_variant; upstream_gene_variant |
rs4764026 |
Chr12:13835420(Fwd) |
intron_variant; upstream_gene_variant |
rs2268107 |
Chr12:13837990(Fwd) |
downstream_gene_variant; intron_variant |
rs995803 |
Chr12:13838475(Fwd) |
downstream_gene_variant; intron_variant |
rs2192977 |
Chr12:13839002(Fwd) |
downstream_gene_variant; intron_variant |
rs2300242 |
Chr12:13840297(Fwd) |
downstream_gene_variant; intron_variant |
rs2300243 |
Chr12:13840419(Fwd) |
downstream_gene_variant; intron_variant |
rs2300244 |
Chr12:13840654(Fwd) |
downstream_gene_variant; intron_variant |
rs170715 |
Chr12:28219423(Fwd) |
|
rs10845826 |
Chr12:13858822(Fwd) |
intron_variant |
rs526490 |
Chr12:28228025(Fwd) |
|
rs11055597 |
Chr12:13862474(Fwd) |
intron_variant |
rs229988 |
Chr12:28218232(Fwd) |
|
rs12231341 |
Chr12:72409436(Fwd) |
intron_variant |
rs2300251 |
Chr12:13861595(Fwd) |
intron_variant |
rs368017 |
Chr12:28226726(Fwd) |
|
rs11179056 |
Chr12:72414171(Fwd) |
intron_variant |
rs2300253 |
Chr12:13861951(Fwd) |
intron_variant |
rs12579303 |
Chr12:28227421(Fwd) |
|
rs12231731 |
Chr12:72380499(Fwd) |
intron_variant |
rs10772705 |
Chr12:13866280(Fwd) |
intron_variant |
rs10843085 |
Chr12:28231087(Fwd) |
|
rs11179041 |
Chr12:72403949(Fwd) |
intron_variant |
rs10772706 |
Chr12:13869689(Fwd) |
intron_variant |
rs10843086 |
Chr12:28231148(Fwd) |
|
rs11179045 |
Chr12:72407403(Fwd) |
intron_variant |
rs2268114 |
Chr12:13867220(Fwd) |
intron_variant |
rs1543297 |
Chr12:28219400(Fwd) |
|
rs6487660 |
Chr12:28222007(Fwd) |
|
rs412736 |
Chr12:28225722(Fwd) |
|
rs11065898 |
Chr12:111862575(Fwd) |
intron_variant; nc_transcript_variant |
rs2073950 |
Chr12:111894072(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2301621 |
Chr12:111895272(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs7134740 |
Chr12:111927739(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs688812 |
Chr12:111962581(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs638791 |
Chr12:111989236(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12317548 |
Chr12:63040598(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant |
rs848132 |
Chr12:111989979(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7135127 |
Chr12:63010175(Fwd) |
downstream_gene_variant |
rs3742003 |
Chr12:111844218(Fwd) |
downstream_gene_variant; intron_variant |
rs12297799 |
Chr12:63040555(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant |
rs12580300 |
Chr12:111849271(Fwd) |
intron_variant |
rs17098139 |
Chr12:63043194(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10849947 |
Chr12:111864684(Fwd) |
intron_variant; nc_transcript_variant |
rs2283358 |
Chr12:111865565(Fwd) |
intron_variant; nc_transcript_variant |
rs7296313 |
Chr12:111878526(Fwd) |
intron_variant; nc_transcript_variant |
rs2239195 |
Chr12:111881309(Fwd) |
intron_variant; nc_transcript_variant |
rs2238154 |
Chr12:111882485(Fwd) |
intron_variant; nc_transcript_variant |
rs739496 |
Chr12:111887659(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs10849949 |
Chr12:111893537(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2301622 |
Chr12:111895203(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs2339816 |
Chr12:111912188(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7965040 |
Chr12:111920295(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1029388 |
Chr12:111926901(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs1607817 |
Chr12:117712186(Fwd) |
intron_variant |
rs6490162 |
Chr12:111941120(Fwd) |
NMD_transcript_variant; intron_variant |
rs2293052 |
Chr12:117715620(Fwd) |
intron_variant |
rs628825 |
Chr12:111951850(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3825102 |
Chr12:117720185(Fwd) |
intron_variant |
rs630512 |
Chr12:111952167(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4767529 |
Chr12:117721812(Fwd) |
intron_variant |
rs657197 |
Chr12:111965658(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7309163 |
Chr12:117729274(Fwd) |
intron_variant |
rs607316 |
Chr12:111969448(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs539291 |
Chr12:117735141(Fwd) |
intron_variant |
rs625093 |
Chr12:111988432(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs530393 |
Chr12:117751258(Fwd) |
intron_variant |
rs616559 |
Chr12:112003350(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs561712 |
Chr12:117752069(Fwd) |
intron_variant |
rs616513 |
Chr12:112003383(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs553715 |
Chr12:117753856(Fwd) |
intron_variant |
rs7398705 |
Chr12:112016016(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs551846 |
Chr12:117754060(Fwd) |
intron_variant |
rs12369009 |
Chr12:112019799(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs549098 |
Chr12:117754327(Fwd) |
intron_variant |
rs10774631 |
Chr12:112023001(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs567581 |
Chr12:117757512(Fwd) |
intron_variant |
rs2239194 |
Chr12:111883779(Fwd) |
downstream_gene_variant; intron_variant |
rs816293 |
Chr12:117762699(Fwd) |
intron_variant |
rs2239197 |
Chr12:111892685(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs570234 |
Chr12:117770982(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4766577 |
Chr12:111894287(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10849952 |
Chr12:111911285(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12230853 |
Chr12:111912584(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1245770 |
Chr12:79775359(Fwd) |
intron_variant; nc_transcript_variant |
rs2285518 |
Chr12:111923417(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1245766 |
Chr12:79776882(Fwd) |
intron_variant; nc_transcript_variant |
rs3815021 |
Chr12:111962692(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12371960 |
Chr12:79778446(Fwd) |
intron_variant; nc_transcript_variant |
rs3858705 |
Chr12:111967002(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6582078 |
Chr12:72374891(Fwd) |
intron_variant |
rs1245778 |
Chr12:79768171(Fwd) |
intron_variant; nc_transcript_variant |
rs11065941 |
Chr12:111972924(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2701566 |
Chr12:79770528(Fwd) |
intron_variant; nc_transcript_variant |
rs1245767 |
Chr12:79776820(Fwd) |
intron_variant; nc_transcript_variant |
rs610769 |
Chr12:111999570(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7971881 |
Chr12:79781339(Fwd) |
feature_truncation; intron_variant; nc_transcript_variant |
rs1245765 |
Chr12:79777291(Fwd) |
intron_variant; nc_transcript_variant |
rs847895 |
Chr12:112118576(Fwd) |
intron_variant |
rs12579420 |
Chr12:79789319(Fwd) |
intron_variant; nc_transcript_variant |
rs1465051 |
Chr12:79778230(Fwd) |
intron_variant; nc_transcript_variant |
rs659964 |
Chr12:112130199(Fwd) |
intron_variant; nc_transcript_variant |
rs4842313 |
Chr12:79895819(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs9788036 |
Chr12:79779307(Fwd) |
intron_variant; nc_transcript_variant |
rs723095 |
Chr12:13836650(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs632650 |
Chr12:112131698(Fwd) |
downstream_gene_variant; intron_variant |
rs1245774 |
Chr12:79760767(Fwd) |
intron_variant; nc_transcript_variant |
rs10778657 |
Chr12:79784735(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2300246 |
Chr12:13841757(Fwd) |
downstream_gene_variant; intron_variant |
rs617044 |
Chr12:112132875(Fwd) |
downstream_gene_variant; intron_variant |
rs1465045 |
Chr12:79788631(Fwd) |
intron_variant; nc_transcript_variant |
rs1465044 |
Chr12:79788930(Fwd) |
intron_variant; nc_transcript_variant |
rs10772700 |
Chr12:13844404(Fwd) |
intron_variant |
rs609230 |
Chr12:112146911(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10778675 |
Chr12:79905558(Fwd) |
|
rs10861975 |
Chr12:79794590(Fwd) |
intron_variant; nc_transcript_variant |
rs2268108 |
Chr12:13838638(Fwd) |
downstream_gene_variant; intron_variant |
rs630616 |
Chr12:112158966(Fwd) |
intron_variant; nc_transcript_variant |
rs7138252 |
Chr12:79922319(Fwd) |
upstream_gene_variant |
rs10861976 |
Chr12:79794658(Fwd) |
intron_variant; nc_transcript_variant |
rs2268109 |
Chr12:13838651(Fwd) |
downstream_gene_variant; intron_variant |
rs7301040 |
Chr12:112025475(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2895728 |
Chr12:79802302(Fwd) |
intron_variant; nc_transcript_variant |
rs2284408 |
Chr12:13842657(Fwd) |
intron_variant |
rs10861941 |
Chr12:79760388(Fwd) |
intron_variant; nc_transcript_variant |
rs2284409 |
Chr12:13842665(Fwd) |
intron_variant |
rs918065 |
Chr12:13842709(Fwd) |
intron_variant |
rs11055586 |
Chr12:13843488(Fwd) |
intron_variant |
rs2284406 |
Chr12:13825416(Fwd) |
intron_variant |
rs2300252 |
Chr12:13861684(Fwd) |
intron_variant |
rs11055593 |
Chr12:13857007(Fwd) |
intron_variant |
rs7968071 |
Chr12:13858116(Fwd) |
intron_variant |
rs7967590 |
Chr12:13858343(Fwd) |
intron_variant |
rs2300255 |
Chr12:13867668(Fwd) |
intron_variant |
rs2300257 |
Chr12:13868507(Fwd) |
intron_variant |
rs10845831 |
Chr12:13871310(Fwd) |
intron_variant |
rs2268118 |
Chr12:13872044(Fwd) |
intron_variant |
rs10845834 |
Chr12:13871636(Fwd) |
intron_variant |
rs11055608 |
Chr12:13913426(Fwd) |
intron_variant |
rs7316902 |
Chr12:13914816(Fwd) |
intron_variant |
rs2284415 |
Chr12:13918091(Fwd) |
intron_variant |
rs1075010 |
Chr12:13918341(Fwd) |
intron_variant |
rs11612284 |
Chr12:13875676(Fwd) |
intron_variant |
rs2268120 |
Chr12:13877888(Fwd) |
intron_variant |
rs10492095 |
Chr12:5561200(Fwd) |
intron_variant; nc_transcript_variant |
rs10845837 |
Chr12:13880168(Fwd) |
intron_variant |
rs17180851 |
Chr12:5554548(Fwd) |
intron_variant; nc_transcript_variant |
rs17821180 |
Chr12:13880509(Fwd) |
intron_variant |
rs10774330 |
Chr12:5557893(Fwd) |
intron_variant; nc_transcript_variant |
rs2300259 |
Chr12:13881556(Fwd) |
intron_variant |
rs10735050 |
Chr12:5558306(Fwd) |
intron_variant; nc_transcript_variant |
rs11179002 |
Chr12:72342284(Fwd) |
NMD_transcript_variant; intron_variant |
rs2300260 |
Chr12:13883684(Fwd) |
intron_variant |
rs17110477 |
Chr12:72343863(Fwd) |
NMD_transcript_variant; intron_variant |
rs2300263 |
Chr12:13899150(Fwd) |
intron_variant |
rs17110489 |
Chr12:72348006(Fwd) |
NMD_transcript_variant; intron_variant |
rs12301788 |
Chr12:13899362(Fwd) |
intron_variant |
rs17110532 |
Chr12:72364668(Fwd) |
intron_variant |
rs10492136 |
Chr12:13911777(Fwd) |
intron_variant |
rs17110536 |
Chr12:72365104(Fwd) |
intron_variant |
rs7307315 |
Chr12:13912682(Fwd) |
intron_variant |
rs17110540 |
Chr12:72365321(Fwd) |
intron_variant |
rs12369725 |
Chr12:13914407(Fwd) |
intron_variant |
rs11178993 |
Chr12:72329142(Fwd) |
upstream_gene_variant |
rs11179023 |
Chr12:72372397(Fwd) |
intron_variant |
rs11055609 |
Chr12:13918248(Fwd) |
intron_variant |
rs11178971 |
Chr12:72261755(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10506645 |
Chr12:72385500(Fwd) |
intron_variant |
rs11055612 |
Chr12:13923328(Fwd) |
intron_variant |
rs3815869 |
Chr12:72290600(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17110627 |
Chr12:72390395(Fwd) |
intron_variant |
rs2268124 |
Chr12:13924583(Fwd) |
intron_variant |
rs7965232 |
Chr12:72296550(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11179033 |
Chr12:72391097(Fwd) |
intron_variant |
rs6488620 |
Chr12:13928463(Fwd) |
intron_variant |
rs11178986 |
Chr12:72312858(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10506646 |
Chr12:72396492(Fwd) |
intron_variant |
rs2300265 |
Chr12:13931441(Fwd) |
intron_variant |
rs17110424 |
Chr12:72314791(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7969114 |
Chr12:72376127(Fwd) |
intron_variant |
rs17110426 |
Chr12:72314982(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4760750 |
Chr12:72377889(Fwd) |
intron_variant |
rs17110432 |
Chr12:72318841(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs11834114 |
Chr12:72394299(Fwd) |
intron_variant |
rs11178988 |
Chr12:72320431(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs11178989 |
Chr12:72320484(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs11178990 |
Chr12:72321850(Fwd) |
downstream_gene_variant |
rs11110899 |
Chr12:102027168(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11178991 |
Chr12:72326894(Fwd) |
|
rs12366302 |
Chr12:102029166(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11178992 |
Chr12:72328238(Fwd) |
upstream_gene_variant |
rs10860758 |
Chr12:102032917(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7963803 |
Chr12:72331318(Fwd) |
upstream_gene_variant |
rs10507134 |
Chr12:102034120(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7954758 |
Chr12:72335794(Fwd) |
NMD_transcript_variant; intron_variant |
rs17031746 |
Chr12:102041757(Fwd) |
intron_variant; nc_transcript_variant |
rs11179001 |
Chr12:72338645(Fwd) |
NMD_transcript_variant; intron_variant |
rs825046 |
Chr12:102044912(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11178996 |
Chr12:72330854(Fwd) |
upstream_gene_variant |
rs3817552 |
Chr12:102045163(Fwd) |
intron_variant; missense_variant; nc_transcript_variant; upstream_gene_variant |
rs7974296 |
Chr12:72285984(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1997205 |
Chr12:102046394(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs6539004 |
Chr12:102056750(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs6539005 |
Chr12:102056826(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2056725 |
Chr12:102057822(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2056724 |
Chr12:102057921(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4764808 |
Chr12:102058750(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1263784 |
Chr12:102071290(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11611478 |
Chr12:102070089(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11110902 |
Chr12:102030703(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs7312925 |
Chr12:71419111(Fwd) |
intron_variant; nc_transcript_variant |
rs7959855 |
Chr12:71425081(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7297408 |
Chr12:26675355(Fwd) |
intron_variant |
rs17109234 |
Chr12:71455700(Fwd) |
intron_variant; nc_transcript_variant |
rs17396348 |
Chr12:26680492(Fwd) |
intron_variant |
rs1798105 |
Chr12:71473534(Fwd) |
intron_variant; nc_transcript_variant |
rs11613811 |
Chr12:26681329(Fwd) |
intron_variant |
rs1705235 |
Chr12:71545273(Fwd) |
intron_variant; nc_transcript_variant |
rs11615475 |
Chr12:26684296(Fwd) |
intron_variant |
rs1798082 |
Chr12:71565311(Fwd) |
intron_variant; nc_transcript_variant |
rs11613431 |
Chr12:26684343(Fwd) |
intron_variant |
rs1397552 |
Chr12:71567331(Fwd) |
intron_variant; nc_transcript_variant |
rs7137796 |
Chr12:26695127(Fwd) |
intron_variant |
rs1705259 |
Chr12:71579613(Fwd) |
intron_variant; nc_transcript_variant |
rs11611069 |
Chr12:26701106(Fwd) |
intron_variant |
rs1355370 |
Chr12:71615183(Fwd) |
intron_variant; nc_transcript_variant |
rs11608490 |
Chr12:26707811(Fwd) |
intron_variant |
rs12814951 |
Chr12:13700576(Fwd) |
downstream_gene_variant |
rs2159100 |
Chr12:2346393(Fwd) |
intron_variant |
rs10879345 |
Chr12:72346800(Fwd) |
NMD_transcript_variant; intron_variant |
rs7960014 |
Chr12:71665876(Fwd) |
intron_variant; nc_transcript_variant |
rs11608578 |
Chr12:26721930(Fwd) |
intron_variant |
rs10772692 |
Chr12:13721148(Fwd) |
intron_variant |
rs4765905 |
Chr12:2349584(Fwd) |
intron_variant |
rs10879346 |
Chr12:72351835(Fwd) |
NMD_transcript_variant; intron_variant |
rs4616134 |
Chr12:71520876(Fwd) |
intron_variant |
rs17397644 |
Chr12:26736660(Fwd) |
intron_variant |
rs4522263 |
Chr12:13712475(Fwd) |
downstream_gene_variant |
rs4765904 |
Chr12:2332393(Fwd) |
intron_variant; nc_transcript_variant |
rs2171363 |
Chr12:72360264(Fwd) |
downstream_gene_variant; intron_variant |
rs17480798 |
Chr12:26878766(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs1806202 |
Chr12:13718561(Fwd) |
intron_variant |
rs769087 |
Chr12:2344644(Fwd) |
intron_variant |
rs7963720 |
Chr12:72366186(Fwd) |
intron_variant |
rs7313538 |
Chr12:26881271(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs1806192 |
Chr12:13719572(Fwd) |
intron_variant |
rs2007044 |
Chr12:2344960(Fwd) |
intron_variant |
rs1843811 |
Chr12:72367474(Fwd) |
intron_variant |
rs17480903 |
Chr12:26883984(Fwd) |
NMD_transcript_variant; intron_variant |
rs2268092 |
Chr12:13721172(Fwd) |
intron_variant |
rs12315711 |
Chr12:2346830(Fwd) |
intron_variant |
rs4760816 |
Chr12:72372601(Fwd) |
intron_variant |
rs1449569 |
Chr12:26911467(Fwd) |
NMD_transcript_variant; intron_variant |
rs1806213 |
Chr12:13723977(Fwd) |
intron_variant |
rs11062170 |
Chr12:2348844(Fwd) |
intron_variant |
rs7309686 |
Chr12:72373854(Fwd) |
intron_variant |
rs11114027 |
Chr12:79775248(Fwd) |
intron_variant; nc_transcript_variant |
rs17820659 |
Chr12:13688908(Fwd) |
intron_variant; nc_transcript_variant |
rs758170 |
Chr12:2361460(Fwd) |
intron_variant |
rs6582073 |
Chr12:72374530(Fwd) |
intron_variant |
rs11114112 |
Chr12:79812829(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12580557 |
Chr12:13692031(Fwd) |
intron_variant; nc_transcript_variant |
rs10774035 |
Chr12:2368674(Fwd) |
intron_variant |
rs6582077 |
Chr12:72374794(Fwd) |
intron_variant |
rs11113980 |
Chr12:79759364(Fwd) |
intron_variant; nc_transcript_variant |
rs12582975 |
Chr12:13692270(Fwd) |
intron_variant; nc_transcript_variant |
rs10774036 |
Chr12:2386948(Fwd) |
intron_variant; nc_transcript_variant |
rs4760817 |
Chr12:72378599(Fwd) |
intron_variant |
rs11113987 |
Chr12:79760464(Fwd) |
intron_variant; nc_transcript_variant |
rs3026173 |
Chr12:13712287(Fwd) |
downstream_gene_variant |
rs10744560 |
Chr12:2387099(Fwd) |
intron_variant; nc_transcript_variant |
rs4641528 |
Chr12:72387342(Fwd) |
intron_variant |
rs11114122 |
Chr12:79847040(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1024582 |
Chr12:2402246(Fwd) |
downstream_gene_variant; intron_variant |
rs4760754 |
Chr12:72388839(Fwd) |
intron_variant |
rs7295198 |
Chr12:79877074(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4298967 |
Chr12:2408194(Fwd) |
intron_variant |
rs4760755 |
Chr12:72389202(Fwd) |
intron_variant |
rs955574 |
Chr12:79903469(Fwd) |
|
rs12424245 |
Chr12:2322513(Fwd) |
intron_variant |
rs7979770 |
Chr12:72393129(Fwd) |
intron_variant |
rs11114143 |
Chr12:79906664(Fwd) |
|
rs11062159 |
Chr12:2326224(Fwd) |
downstream_gene_variant; intron_variant |
rs1532008 |
Chr12:72390964(Fwd) |
intron_variant |
rs11114145 |
Chr12:79908214(Fwd) |
|
rs11062161 |
Chr12:2329970(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs2368049 |
Chr12:72391999(Fwd) |
intron_variant |
rs11114146 |
Chr12:79908350(Fwd) |
|
rs10774034 |
Chr12:2330458(Fwd) |
intron_variant; nc_transcript_variant |
rs12319219 |
Chr12:72370085(Fwd) |
intron_variant |
rs11114148 |
Chr12:79908635(Fwd) |
|
rs10848642 |
Chr12:2331572(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs11179027 |
Chr12:72377312(Fwd) |
intron_variant |
rs1553525 |
Chr12:79911687(Fwd) |
|
rs11062162 |
Chr12:2332104(Fwd) |
intron_variant; nc_transcript_variant |
rs12229394 |
Chr12:72392914(Fwd) |
intron_variant |
rs10861990 |
Chr12:79918022(Fwd) |
downstream_gene_variant |
rs1108221 |
Chr12:2332795(Fwd) |
intron_variant; upstream_gene_variant |
rs10879350 |
Chr12:72393575(Fwd) |
intron_variant |
rs17229687 |
Chr12:79922925(Fwd) |
upstream_gene_variant |
rs1108222 |
Chr12:2332856(Fwd) |
intron_variant; upstream_gene_variant |
rs11834097 |
Chr12:72394282(Fwd) |
intron_variant |
rs7308762 |
Chr12:79931070(Fwd) |
upstream_gene_variant |
rs1108074 |
Chr12:2333484(Fwd) |
intron_variant; upstream_gene_variant |
rs11114174 |
Chr12:79958118(Fwd) |
|
rs1108073 |
Chr12:2333638(Fwd) |
intron_variant; upstream_gene_variant |
rs7954927 |
Chr12:79798573(Fwd) |
intron_variant; nc_transcript_variant |
rs7297582 |
Chr12:2355806(Fwd) |
intron_variant |
rs11114107 |
Chr12:79799216(Fwd) |
intron_variant; nc_transcript_variant |
rs2370414 |
Chr12:2368396(Fwd) |
intron_variant |
rs17294719 |
Chr12:79812271(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2239038 |
Chr12:2374130(Fwd) |
intron_variant; upstream_gene_variant |
rs11114116 |
Chr12:79831956(Fwd) |
intron_variant; nc_transcript_variant |
rs4765914 |
Chr12:2420377(Fwd) |
intron_variant |
rs7315113 |
Chr12:79832584(Fwd) |
intron_variant; nc_transcript_variant |
rs10774037 |
Chr12:2420526(Fwd) |
intron_variant |
rs7135647 |
Chr12:79839153(Fwd) |
intron_variant; nc_transcript_variant |
rs1386489 |
Chr12:72349290(Fwd) |
NMD_transcript_variant; intron_variant |
rs11614604 |
Chr12:72503687(Fwd) |
intron_variant; nc_transcript_variant |
rs10849276 |
Chr12:5594103(Fwd) |
intron_variant; nc_transcript_variant |
rs11114133 |
Chr12:79885077(Fwd) |
intron_variant; nc_transcript_variant |
rs10784944 |
Chr12:72359418(Fwd) |
downstream_gene_variant; intron_variant |
rs11179071 |
Chr12:72455185(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11063708 |
Chr12:5594403(Fwd) |
intron_variant; nc_transcript_variant |
rs12227728 |
Chr12:79923540(Fwd) |
upstream_gene_variant |
rs4760751 |
Chr12:72377918(Fwd) |
intron_variant |
rs1487283 |
Chr12:72468040(Fwd) |
intron_variant; nc_transcript_variant |
rs3924027 |
Chr12:5595435(Fwd) |
intron_variant; nc_transcript_variant |
rs12229260 |
Chr12:79957172(Fwd) |
downstream_gene_variant |
rs1487281 |
Chr12:72380022(Fwd) |
intron_variant |
rs4760822 |
Chr12:72479611(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7965477 |
Chr12:5595747(Fwd) |
intron_variant; nc_transcript_variant |
rs1386490 |
Chr12:72349371(Fwd) |
NMD_transcript_variant; intron_variant |
rs3858589 |
Chr12:72499323(Fwd) |
intron_variant; nc_transcript_variant |
rs4077470 |
Chr12:5596812(Fwd) |
intron_variant; nc_transcript_variant |
rs7968346 |
Chr12:72349841(Fwd) |
NMD_transcript_variant; intron_variant |
rs4930820 |
Chr12:5597205(Fwd) |
intron_variant; nc_transcript_variant |
rs10784942 |
Chr12:72351860(Fwd) |
NMD_transcript_variant; intron_variant |
rs11063703 |
Chr12:5589409(Fwd) |
intron_variant; nc_transcript_variant |
rs4760749 |
Chr12:72352108(Fwd) |
NMD_transcript_variant; intron_variant |
rs11063707 |
Chr12:5594325(Fwd) |
intron_variant; nc_transcript_variant |
rs7299582 |
Chr12:72356314(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; intron_variant |
rs6489628 |
Chr12:5596346(Fwd) |
intron_variant; nc_transcript_variant |
rs1843812 |
Chr12:72367655(Fwd) |
intron_variant |
rs7301972 |
Chr12:5596454(Fwd) |
intron_variant; nc_transcript_variant |
rs2367899 |
Chr12:72369165(Fwd) |
intron_variant |
rs10161033 |
Chr12:5599646(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10748189 |
Chr12:72376715(Fwd) |
intron_variant |
rs7484401 |
Chr12:5599902(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7300490 |
Chr12:72377683(Fwd) |
intron_variant |
rs7485608 |
Chr12:5589291(Fwd) |
intron_variant; nc_transcript_variant |
rs2046582 |
Chr12:72380305(Fwd) |
intron_variant |
rs990234 |
Chr12:72398117(Fwd) |
intron_variant |
rs1473473 |
Chr12:72404378(Fwd) |
intron_variant |
rs17005544 |
Chr12:79785690(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17005546 |
Chr12:79790026(Fwd) |
intron_variant; nc_transcript_variant |
rs9132 |
Chr12:104166243(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs4578461 |
Chr12:79790779(Fwd) |
intron_variant; nc_transcript_variant |
rs10861096 |
Chr12:104169356(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant |
rs12581451 |
Chr12:79791607(Fwd) |
intron_variant; nc_transcript_variant |
rs10861097 |
Chr12:104170474(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs10506815 |
Chr12:79793312(Fwd) |
intron_variant; nc_transcript_variant |
rs3751204 |
Chr12:104171455(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant |
rs1405493 |
Chr12:79793964(Fwd) |
intron_variant; nc_transcript_variant |
rs954921 |
Chr12:104173630(Fwd) |
NMD_transcript_variant; intron_variant |
rs11608780 |
Chr12:79795919(Fwd) |
intron_variant; nc_transcript_variant |
rs10861099 |
Chr12:104175575(Fwd) |
NMD_transcript_variant; intron_variant |
rs11608808 |
Chr12:79796144(Fwd) |
intron_variant; nc_transcript_variant |
rs4964820 |
Chr12:104182857(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs1465046 |
Chr12:79797095(Fwd) |
intron_variant; nc_transcript_variant |
rs1370777 |
Chr12:104183358(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs7303658 |
Chr12:79797902(Fwd) |
intron_variant; nc_transcript_variant |
rs934843 |
Chr12:104185132(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs7133421 |
Chr12:79798167(Fwd) |
intron_variant; nc_transcript_variant |
rs934847 |
Chr12:104185693(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1465047 |
Chr12:79798317(Fwd) |
intron_variant; nc_transcript_variant |
rs1866294 |
Chr12:104186795(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1465048 |
Chr12:79798409(Fwd) |
intron_variant; nc_transcript_variant |
rs1866295 |
Chr12:104186946(Fwd) |
NMD_transcript_variant; downstream_gene_variant; synonymous_variant; upstream_gene_variant |
rs1465049 |
Chr12:79798494(Fwd) |
intron_variant; nc_transcript_variant |
rs11111781 |
Chr12:104187440(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |