rs_ID |
Location |
Functional Annotation |
rs10198215 |
Chr2:239165909(Fwd) |
downstream_gene_variant; intron_variant |
rs6750890 |
Chr2:209011014(Fwd) |
upstream_gene_variant |
rs3100584 |
Chr2:232946290(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1972874 |
Chr2:239178402(Fwd) |
intron_variant |
rs11679871 |
Chr2:208977323(Fwd) |
upstream_gene_variant |
rs3116158 |
Chr2:232955363(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11892306 |
Chr2:239188479(Fwd) |
intron_variant; upstream_gene_variant |
rs3100591 |
Chr2:232968846(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11892309 |
Chr2:239188493(Fwd) |
intron_variant; upstream_gene_variant |
rs3103268 |
Chr2:232984969(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6754875 |
Chr2:239193219(Fwd) |
downstream_gene_variant; intron_variant |
rs1869457 |
Chr2:232989793(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs13002160 |
Chr2:239202131(Fwd) |
upstream_gene_variant |
rs3103261 |
Chr2:232993574(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs3100624 |
Chr2:232938583(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1427339 |
Chr2:108588292(Fwd) |
|
rs11685873 |
Chr2:108611519(Fwd) |
intron_variant |
rs3731684 |
Chr2:108618514(Fwd) |
intron_variant |
rs11681633 |
Chr2:108654188(Fwd) |
|
rs1992248 |
Chr2:120283173(Fwd) |
upstream_gene_variant |
rs2587686 |
Chr2:120285695(Fwd) |
upstream_gene_variant |
rs2579618 |
Chr2:120288463(Fwd) |
|
rs4600662 |
Chr2:123567065(Fwd) |
|
rs2587683 |
Chr2:120292249(Fwd) |
|
rs17463862 |
Chr2:123581116(Fwd) |
|
rs2579621 |
Chr2:120294700(Fwd) |
|
rs17366709 |
Chr2:123583790(Fwd) |
|
rs2587653 |
Chr2:120298231(Fwd) |
upstream_gene_variant |
rs17463966 |
Chr2:123598782(Fwd) |
|
rs2579623 |
Chr2:120298350(Fwd) |
upstream_gene_variant |
rs17008754 |
Chr2:123603320(Fwd) |
|
rs2587654 |
Chr2:120299172(Fwd) |
upstream_gene_variant |
rs17008771 |
Chr2:123606874(Fwd) |
|
rs2579624 |
Chr2:120303820(Fwd) |
5_prime_UTR_variant; NMD_transcript_variant; missense_variant |
rs7609162 |
Chr2:123610375(Fwd) |
|
rs2587710 |
Chr2:120311479(Fwd) |
NMD_transcript_variant; intron_variant |
rs17367160 |
Chr2:123653197(Fwd) |
|
rs2920695 |
Chr2:120318903(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17367270 |
Chr2:123664879(Fwd) |
|
rs2587706 |
Chr2:120323261(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17367528 |
Chr2:123694166(Fwd) |
|
rs2579626 |
Chr2:120309123(Fwd) |
NMD_transcript_variant; intron_variant |
rs17367563 |
Chr2:123697781(Fwd) |
|
rs1609223 |
Chr2:123699220(Fwd) |
|
rs10496603 |
Chr2:123716681(Fwd) |
|
rs17367752 |
Chr2:123719406(Fwd) |
|
rs7349363 |
Chr2:123726800(Fwd) |
|
rs9653409 |
Chr2:123738869(Fwd) |
|
rs17367971 |
Chr2:123743252(Fwd) |
|
rs17465214 |
Chr2:123749141(Fwd) |
|
rs1016386 |
Chr2:123758464(Fwd) |
|
rs13419980 |
Chr2:239140682(Fwd) |
nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs2166720 |
Chr2:61577435(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; synonymous_variant; upstream_gene_variant |
rs1527972 |
Chr2:123660810(Fwd) |
|
rs10201361 |
Chr2:239173905(Fwd) |
intron_variant; upstream_gene_variant |
rs988911 |
Chr2:61607510(Fwd) |
NMD_transcript_variant; intron_variant |
rs10496093 |
Chr2:61618660(Fwd) |
NMD_transcript_variant; intron_variant |
rs6717124 |
Chr2:61614075(Fwd) |
NMD_transcript_variant; intron_variant |
rs2034311 |
Chr2:61623548(Fwd) |
NMD_transcript_variant; intron_variant |
rs7559099 |
Chr2:61631390(Fwd) |
NMD_transcript_variant; intron_variant |
rs778754 |
Chr2:61780230(Fwd) |
upstream_gene_variant |
rs17008940 |
Chr2:61618598(Fwd) |
NMD_transcript_variant; intron_variant |
rs4387777 |
Chr2:61629635(Fwd) |
NMD_transcript_variant; intron_variant |
rs7603751 |
Chr2:61641785(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs17007967 |
Chr2:61512760(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17007989 |
Chr2:61513449(Fwd) |
intron_variant; nc_transcript_variant |
rs2123113 |
Chr2:61517471(Fwd) |
intron_variant; nc_transcript_variant |
rs17008097 |
Chr2:61523070(Fwd) |
intron_variant; nc_transcript_variant |
rs1584300 |
Chr2:61586001(Fwd) |
NMD_transcript_variant; intron_variant |
rs1584301 |
Chr2:61586132(Fwd) |
NMD_transcript_variant; intron_variant |
rs17008755 |
Chr2:61604429(Fwd) |
NMD_transcript_variant; intron_variant |
rs13410306 |
Chr2:61658685(Fwd) |
NMD_transcript_variant; intron_variant |
rs3108986 |
Chr2:130360682(Fwd) |
|
rs3109306 |
Chr2:130362926(Fwd) |
|
rs3109308 |
Chr2:130363121(Fwd) |
|
rs3109303 |
Chr2:130355506(Fwd) |
|
rs3108988 |
Chr2:130358654(Fwd) |
|
rs3109305 |
Chr2:130359779(Fwd) |
|
rs3094425 |
Chr2:130360890(Fwd) |
|
rs13391055 |
Chr2:130371477(Fwd) |
|
rs13412058 |
Chr2:130379165(Fwd) |
|
rs17049589 |
Chr2:130322766(Fwd) |
|
rs4426564 |
Chr2:96780986(Fwd) |
synonymous_variant |
rs17049594 |
Chr2:130323472(Fwd) |
|
rs1168965 |
Chr2:96787899(Fwd) |
downstream_gene_variant |
rs2406989 |
Chr2:130324894(Fwd) |
|
rs1168968 |
Chr2:96825363(Fwd) |
|
rs17049608 |
Chr2:130336183(Fwd) |
|
rs2692954 |
Chr2:96683378(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17049620 |
Chr2:130344037(Fwd) |
|
rs2969475 |
Chr2:96685021(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17049621 |
Chr2:130344073(Fwd) |
|
rs2579515 |
Chr2:96686723(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4662967 |
Chr2:130347850(Fwd) |
|
rs2579552 |
Chr2:96737083(Fwd) |
|
rs4662968 |
Chr2:130354577(Fwd) |
|
rs2579550 |
Chr2:96741944(Fwd) |
|
rs916800 |
Chr2:130356031(Fwd) |
|
rs2692936 |
Chr2:96745729(Fwd) |
|
rs1859062 |
Chr2:130381377(Fwd) |
|
rs2692893 |
Chr2:96756547(Fwd) |
|
rs3109015 |
Chr2:130384917(Fwd) |
|
rs13019188 |
Chr2:96774199(Fwd) |
downstream_gene_variant |
rs17049591 |
Chr2:130323075(Fwd) |
|
rs10183151 |
Chr2:96774786(Fwd) |
downstream_gene_variant |
rs7604842 |
Chr2:96777340(Fwd) |
downstream_gene_variant |
rs4907299 |
Chr2:96780122(Fwd) |
3_prime_UTR_variant |
rs2229169 |
Chr2:96780716(Fwd) |
synonymous_variant |
rs2692894 |
Chr2:96784934(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs893173 |
Chr2:96789787(Fwd) |
synonymous_variant |
rs2969491 |
Chr2:96794982(Fwd) |
downstream_gene_variant; intron_variant |
rs1657502 |
Chr2:96795608(Fwd) |
downstream_gene_variant; missense_variant |
rs7592624 |
Chr2:234602906(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs749459 |
Chr2:96795714(Fwd) |
downstream_gene_variant; synonymous_variant |
rs12988520 |
Chr2:234607394(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs749457 |
Chr2:96795944(Fwd) |
downstream_gene_variant; intron_variant |
rs4663871 |
Chr2:234581587(Fwd) |
intron_variant |
rs1168976 |
Chr2:96813480(Fwd) |
upstream_gene_variant |
rs17862857 |
Chr2:234582084(Fwd) |
intron_variant |
rs1168975 |
Chr2:96814075(Fwd) |
upstream_gene_variant |
rs4663877 |
Chr2:234586671(Fwd) |
intron_variant; upstream_gene_variant |
rs1369296 |
Chr2:50232325(Fwd) |
intron_variant |
rs1168974 |
Chr2:96814928(Fwd) |
upstream_gene_variant |
rs12053462 |
Chr2:234587639(Fwd) |
intron_variant; upstream_gene_variant |
rs1363051 |
Chr2:50279475(Fwd) |
intron_variant |
rs1168970 |
Chr2:96816606(Fwd) |
upstream_gene_variant |
rs12474215 |
Chr2:234589560(Fwd) |
intron_variant; upstream_gene_variant |
rs11680950 |
Chr2:96844981(Fwd) |
|
rs12472689 |
Chr2:234589616(Fwd) |
intron_variant; upstream_gene_variant |
rs3821051 |
Chr2:96912787(Fwd) |
downstream_gene_variant |
rs28946877 |
Chr2:234590243(Fwd) |
intron_variant; upstream_gene_variant |
rs2301707 |
Chr2:96931846(Fwd) |
upstream_gene_variant |
rs17864686 |
Chr2:234591339(Fwd) |
intron_variant; synonymous_variant |
rs772175 |
Chr2:96944553(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant |
rs17868325 |
Chr2:234594387(Fwd) |
intron_variant |
rs772178 |
Chr2:96963684(Fwd) |
intron_variant |
rs6753317 |
Chr2:234594979(Fwd) |
intron_variant |
rs4144055 |
Chr2:96647856(Fwd) |
NMD_transcript_variant; intron_variant |
rs4485562 |
Chr2:234597566(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs11687113 |
Chr2:96658588(Fwd) |
upstream_gene_variant |
rs12474980 |
Chr2:234600116(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs2579520 |
Chr2:96660300(Fwd) |
upstream_gene_variant |
rs12476197 |
Chr2:234601224(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1917890 |
Chr2:96672001(Fwd) |
upstream_gene_variant |
rs12466747 |
Chr2:234606787(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2579519 |
Chr2:96675166(Fwd) |
upstream_gene_variant |
rs12471030 |
Chr2:234607560(Fwd) |
NMD_transcript_variant; feature_truncation; intron_variant; nc_transcript_variant |
rs2969490 |
Chr2:96803904(Fwd) |
intron_variant; upstream_gene_variant |
rs7420193 |
Chr2:234611523(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2438978 |
Chr2:96679740(Fwd) |
intron_variant; nc_transcript_variant |
rs4663326 |
Chr2:234616571(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10164580 |
Chr2:79882996(Fwd) |
intron_variant |
rs2885295 |
Chr2:234619866(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13411356 |
Chr2:79883983(Fwd) |
intron_variant |
rs28898596 |
Chr2:234620640(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1511198 |
Chr2:79884445(Fwd) |
intron_variant |
rs3893334 |
Chr2:234620917(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1159418 |
Chr2:79885114(Fwd) |
intron_variant |
rs2013030 |
Chr2:234621040(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12620274 |
Chr2:79888572(Fwd) |
intron_variant |
rs2013021 |
Chr2:234621086(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10190617 |
Chr2:79893775(Fwd) |
intron_variant |
rs2013018 |
Chr2:234621157(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13394943 |
Chr2:79894884(Fwd) |
intron_variant |
rs4556969 |
Chr2:234621404(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17017476 |
Chr2:79897781(Fwd) |
intron_variant |
rs3755321 |
Chr2:234621825(Fwd) |
NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant; upstream_gene_variant |
rs1533123 |
Chr2:79898937(Fwd) |
intron_variant |
rs12475068 |
Chr2:234622110(Fwd) |
NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs1533122 |
Chr2:79899193(Fwd) |
intron_variant |
rs3892170 |
Chr2:234622412(Fwd) |
NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
rs17017500 |
Chr2:79899436(Fwd) |
intron_variant |
rs17862870 |
Chr2:234622742(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11677138 |
Chr2:122732830(Fwd) |
|
rs4380187 |
Chr2:185811940(Fwd) |
|
rs4663945 |
Chr2:234623117(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4430964 |
Chr2:122762195(Fwd) |
|
rs17584522 |
Chr2:185681730(Fwd) |
intron_variant |
rs12477216 |
Chr2:234623667(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17779391 |
Chr2:122776465(Fwd) |
|
rs7593816 |
Chr2:185782312(Fwd) |
intron_variant |
rs17868334 |
Chr2:234624817(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4848168 |
Chr2:122809849(Fwd) |
|
rs17584976 |
Chr2:185926285(Fwd) |
|
rs17863791 |
Chr2:234624884(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17863792 |
Chr2:234625126(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17874943 |
Chr2:234625239(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs28898605 |
Chr2:234625494(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3806595 |
Chr2:234625718(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3806594 |
Chr2:234625890(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3806593 |
Chr2:234625919(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3806591 |
Chr2:234626199(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3732221 |
Chr2:234627010(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3732220 |
Chr2:234627048(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3732218 |
Chr2:234627304(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs904855 |
Chr2:234628576(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs904856 |
Chr2:234628647(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12466779 |
Chr2:234628694(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12463641 |
Chr2:234628715(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12468356 |
Chr2:234628747(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12468543 |
Chr2:234629239(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs28899186 |
Chr2:234629585(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10929293 |
Chr2:234630186(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs12479208 |
Chr2:234630900(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs28899187 |
Chr2:234630967(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs28898615 |
Chr2:234631007(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs28899189 |
Chr2:234634324(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs28898621 |
Chr2:234639211(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4663964 |
Chr2:234650236(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs3796088 |
Chr2:234651800(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs4663968 |
Chr2:234655144(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12466997 |
Chr2:234656517(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs17863798 |
Chr2:234656735(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17862878 |
Chr2:234661948(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs12052787 |
Chr2:234666581(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs2003569 |
Chr2:234667937(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs17864705 |
Chr2:234672328(Fwd) |
NMD_transcript_variant; intron_variant |
rs3771342 |
Chr2:234672663(Fwd) |
NMD_transcript_variant; intron_variant |
rs17868342 |
Chr2:234673516(Fwd) |
NMD_transcript_variant; intron_variant |
rs12479045 |
Chr2:234673588(Fwd) |
NMD_transcript_variant; intron_variant |
rs1018124 |
Chr2:234676118(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs6751673 |
Chr2:234604903(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1604144 |
Chr2:234605835(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4663325 |
Chr2:234616357(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4663327 |
Chr2:234617632(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4233633 |
Chr2:234619937(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1534260 |
Chr2:156894544(Fwd) |
upstream_gene_variant |
rs2882618 |
Chr2:156893877(Fwd) |
upstream_gene_variant |
rs11680065 |
Chr2:156862613(Fwd) |
|
rs4664790 |
Chr2:156867747(Fwd) |
downstream_gene_variant |
rs6748811 |
Chr2:156877774(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs1110075 |
Chr2:156885363(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs7570959 |
Chr2:156885750(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs1918173 |
Chr2:156893605(Fwd) |
upstream_gene_variant |
rs2289355 |
Chr2:42981990(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs1371657 |
Chr2:198966789(Fwd) |
NMD_transcript_variant; intron_variant |
rs1534261 |
Chr2:156894018(Fwd) |
upstream_gene_variant |
rs7578904 |
Chr2:42984490(Fwd) |
downstream_gene_variant |
rs1440084 |
Chr2:198961065(Fwd) |
NMD_transcript_variant; intron_variant |
rs2177952 |
Chr2:156895806(Fwd) |
|
rs333228 |
Chr2:108631051(Fwd) |
downstream_gene_variant |
rs7566714 |
Chr2:42984707(Fwd) |
downstream_gene_variant |
rs6430407 |
Chr2:134039363(Fwd) |
intron_variant; nc_transcript_variant |
rs1036336 |
Chr2:198964120(Fwd) |
NMD_transcript_variant; intron_variant |
rs7371289 |
Chr2:156878675(Fwd) |
intron_variant; nc_transcript_variant |
rs333231 |
Chr2:108635697(Fwd) |
|
rs4953653 |
Chr2:42989159(Fwd) |
downstream_gene_variant |
rs1549739 |
Chr2:134044803(Fwd) |
downstream_gene_variant; intron_variant |
rs3755330 |
Chr2:198959372(Fwd) |
NMD_transcript_variant; intron_variant |
rs10496417 |
Chr2:108631729(Fwd) |
downstream_gene_variant |
rs2278582 |
Chr2:42989444(Fwd) |
downstream_gene_variant |
rs1344726 |
Chr2:134046163(Fwd) |
downstream_gene_variant; intron_variant |
rs3755333 |
Chr2:198959603(Fwd) |
NMD_transcript_variant; intron_variant |
rs2278584 |
Chr2:42989744(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs1367207 |
Chr2:134035868(Fwd) |
intron_variant; nc_transcript_variant |
rs1946645 |
Chr2:198961389(Fwd) |
NMD_transcript_variant; intron_variant |
rs1992286 |
Chr2:42990336(Fwd) |
downstream_gene_variant; synonymous_variant |
rs1985935 |
Chr2:134028503(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs3771361 |
Chr2:198962784(Fwd) |
NMD_transcript_variant; intron_variant |
rs1971138 |
Chr2:42969270(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1430170 |
Chr2:134033399(Fwd) |
intron_variant; nc_transcript_variant |
rs3771362 |
Chr2:198962831(Fwd) |
NMD_transcript_variant; intron_variant |
rs4953631 |
Chr2:42970990(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2115866 |
Chr2:133999831(Fwd) |
intron_variant |
rs1036335 |
Chr2:198964009(Fwd) |
NMD_transcript_variant; intron_variant |
rs1016607 |
Chr2:42971687(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4057049 |
Chr2:134019065(Fwd) |
intron_variant; upstream_gene_variant |
rs2009631 |
Chr2:198964380(Fwd) |
NMD_transcript_variant; intron_variant |
rs6713059 |
Chr2:42977280(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7568471 |
Chr2:134016435(Fwd) |
intron_variant |
rs986534 |
Chr2:198965338(Fwd) |
NMD_transcript_variant; intron_variant |
rs6544594 |
Chr2:42977579(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2880366 |
Chr2:198965495(Fwd) |
NMD_transcript_variant; intron_variant |
rs7591304 |
Chr2:42977799(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs3732231 |
Chr2:198966257(Fwd) |
NMD_transcript_variant; intron_variant |
rs6544595 |
Chr2:42977870(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12693831 |
Chr2:198967289(Fwd) |
NMD_transcript_variant; intron_variant |
rs4953636 |
Chr2:42980069(Fwd) |
NMD_transcript_variant; feature_truncation; intron_variant; nc_transcript_variant |
rs7603309 |
Chr2:198979763(Fwd) |
NMD_transcript_variant; intron_variant |
rs965374 |
Chr2:42993166(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs6433953 |
Chr2:182911702(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1196185 |
Chr2:182884959(Fwd) |
intron_variant; nc_transcript_variant |
rs13003589 |
Chr2:182887596(Fwd) |
intron_variant; nc_transcript_variant |
rs12693291 |
Chr2:182887637(Fwd) |
intron_variant; nc_transcript_variant |
rs1196183 |
Chr2:182888983(Fwd) |
intron_variant; nc_transcript_variant |
rs6747855 |
Chr2:182904822(Fwd) |
intron_variant; nc_transcript_variant |
rs4666807 |
Chr2:182907386(Fwd) |
intron_variant; nc_transcript_variant |
rs12617778 |
Chr2:182907978(Fwd) |
intron_variant; nc_transcript_variant |
rs2701664 |
Chr2:182908664(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2701665 |
Chr2:182908768(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1913896 |
Chr2:182911996(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs16822401 |
Chr2:182912952(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs16822409 |
Chr2:182913234(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs16822412 |
Chr2:182914278(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs3892365 |
Chr2:239163216(Fwd) |
intron_variant; nc_transcript_variant |
rs1400009 |
Chr2:182915414(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs744837 |
Chr2:239163744(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs1400010 |
Chr2:182915502(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2304676 |
Chr2:239179914(Fwd) |
downstream_gene_variant; intron_variant |
rs1196155 |
Chr2:182921272(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7570188 |
Chr2:239172863(Fwd) |
intron_variant; upstream_gene_variant |
rs12693292 |
Chr2:182921723(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1196157 |
Chr2:182925120(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1196160 |
Chr2:182928012(Fwd) |
intron_variant; nc_transcript_variant |
rs13017711 |
Chr2:182930275(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1196167 |
Chr2:182932398(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11681208 |
Chr2:42987268(Fwd) |
downstream_gene_variant |
rs10185815 |
Chr2:42973439(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs13389948 |
Chr2:42974576(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10205149 |
Chr2:42977733(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs930420 |
Chr2:42978436(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs272064 |
Chr2:116612503(Fwd) |
|
rs272055 |
Chr2:116616776(Fwd) |
|
rs272054 |
Chr2:116617425(Fwd) |
|
rs272043 |
Chr2:116625784(Fwd) |
|
rs272032 |
Chr2:116640033(Fwd) |
|
rs272017 |
Chr2:116646175(Fwd) |
|
rs7578843 |
Chr2:116669201(Fwd) |
|
rs13024433 |
Chr2:225774612(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7569451 |
Chr2:116669314(Fwd) |
|
rs11692992 |
Chr2:225786905(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs272068 |
Chr2:116609440(Fwd) |
|
rs17271567 |
Chr2:225795103(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs775335 |
Chr2:116662309(Fwd) |
|
rs10498171 |
Chr2:225796610(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs272041 |
Chr2:116628788(Fwd) |
|
rs10498172 |
Chr2:225797167(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4557005 |
Chr2:1919696(Fwd) |
intron_variant; upstream_gene_variant |
rs971563 |
Chr2:60774773(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs272031 |
Chr2:116640157(Fwd) |
|
rs13021690 |
Chr2:225814772(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1432539 |
Chr2:1919847(Fwd) |
intron_variant; upstream_gene_variant |
rs2556376 |
Chr2:60760032(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs272030 |
Chr2:116640293(Fwd) |
|
rs17271608 |
Chr2:225809239(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7588882 |
Chr2:1931058(Fwd) |
intron_variant |
rs2556377 |
Chr2:60760637(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs272029 |
Chr2:116640375(Fwd) |
|
rs13021295 |
Chr2:225811581(Fwd) |
NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
rs3748989 |
Chr2:1946968(Fwd) |
synonymous_variant |
rs3771270 |
Chr2:60769455(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs272020 |
Chr2:116644461(Fwd) |
|
rs13016818 |
Chr2:225786329(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6722043 |
Chr2:1950521(Fwd) |
intron_variant |
rs6739994 |
Chr2:60770454(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10498170 |
Chr2:225792317(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6548052 |
Chr2:1951082(Fwd) |
intron_variant |
rs2665668 |
Chr2:60768978(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs13018710 |
Chr2:225793447(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs919718 |
Chr2:1952576(Fwd) |
intron_variant |
rs2679178 |
Chr2:232797861(Fwd) |
|
rs1395914 |
Chr2:225797959(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11695699 |
Chr2:1954444(Fwd) |
intron_variant |
rs749052 |
Chr2:232796610(Fwd) |
|
rs10498174 |
Chr2:225800172(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11127299 |
Chr2:1961787(Fwd) |
intron_variant |
rs2580818 |
Chr2:232802303(Fwd) |
|
rs953945 |
Chr2:225801484(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs3934844 |
Chr2:1878679(Fwd) |
intron_variant |
rs2580821 |
Chr2:232804155(Fwd) |
|
rs17199431 |
Chr2:225810943(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12472983 |
Chr2:1881964(Fwd) |
intron_variant |
rs2679165 |
Chr2:232820979(Fwd) |
upstream_gene_variant |
rs12999154 |
Chr2:225824421(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11127306 |
Chr2:1887049(Fwd) |
downstream_gene_variant; intron_variant |
rs2679166 |
Chr2:232821729(Fwd) |
upstream_gene_variant |
rs11679104 |
Chr2:225830996(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11127305 |
Chr2:1902562(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17199740 |
Chr2:232828967(Fwd) |
NMD_transcript_variant; intron_variant |
rs7569781 |
Chr2:225831586(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs13016585 |
Chr2:1934252(Fwd) |
intron_variant |
rs3116154 |
Chr2:232857909(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6731100 |
Chr2:225774390(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2195903 |
Chr2:1907446(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3116162 |
Chr2:232860077(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6731109 |
Chr2:225774413(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7569044 |
Chr2:1951254(Fwd) |
intron_variant |
rs2342296 |
Chr2:232869025(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1857996 |
Chr2:225806764(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12463771 |
Chr2:208996214(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs3100601 |
Chr2:232871232(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6744132 |
Chr2:239144542(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12464552 |
Chr2:209002060(Fwd) |
nc_transcript_variant; non_coding_exon_variant |
rs3116236 |
Chr2:232912325(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6431590 |
Chr2:239165128(Fwd) |
downstream_gene_variant; intron_variant |
rs12468692 |
Chr2:209002111(Fwd) |
nc_transcript_variant; non_coding_exon_variant |
rs3100616 |
Chr2:232913682(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |