rs_ID |
Location |
Functional Annotation |
rs974293 |
Chr17:44150233(Fwd) |
intron_variant; nc_transcript_variant |
rs1117253 |
Chr17:44149297(Fwd) |
intron_variant; nc_transcript_variant |
rs17659731 |
Chr17:44144634(Fwd) |
intron_variant; nc_transcript_variant |
rs17575850 |
Chr17:44144387(Fwd) |
intron_variant; nc_transcript_variant |
rs1476554 |
Chr17:44159102(Fwd) |
intron_variant; nc_transcript_variant |
rs17659881 |
Chr17:44157597(Fwd) |
intron_variant; nc_transcript_variant |
rs2316954 |
Chr17:44156167(Fwd) |
intron_variant; nc_transcript_variant |
rs2066899 |
Chr17:44155732(Fwd) |
intron_variant; nc_transcript_variant |
rs8080583 |
Chr17:44162597(Fwd) |
intron_variant; nc_transcript_variant |
rs17660065 |
Chr17:44162284(Fwd) |
intron_variant; nc_transcript_variant |
rs17660017 |
Chr17:44160674(Fwd) |
intron_variant; nc_transcript_variant |
rs17659953 |
Chr17:44159725(Fwd) |
intron_variant; nc_transcript_variant |
rs17660251 |
Chr17:44166646(Fwd) |
intron_variant; nc_transcript_variant |
rs17660167 |
Chr17:44166311(Fwd) |
intron_variant; nc_transcript_variant |
rs17660132 |
Chr17:44165803(Fwd) |
intron_variant; nc_transcript_variant |
rs3912061 |
Chr17:44165098(Fwd) |
intron_variant; nc_transcript_variant |
rs17575423 |
Chr17:44129253(Fwd) |
intron_variant; nc_transcript_variant |
rs17575437 |
Chr17:44133031(Fwd) |
intron_variant; nc_transcript_variant |
rs12150064 |
Chr17:44128407(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17653836 |
Chr17:44128876(Fwd) |
intron_variant; nc_transcript_variant |
rs17575507 |
Chr17:44134095(Fwd) |
intron_variant; nc_transcript_variant |
rs876944 |
Chr17:44134391(Fwd) |
intron_variant; nc_transcript_variant |
rs17653889 |
Chr17:44133070(Fwd) |
intron_variant; nc_transcript_variant |
rs17653906 |
Chr17:44133142(Fwd) |
intron_variant; nc_transcript_variant |
rs17653998 |
Chr17:44135985(Fwd) |
intron_variant; nc_transcript_variant |
rs41384744 |
Chr17:44137070(Fwd) |
intron_variant; nc_transcript_variant |
rs1107820 |
Chr17:44135359(Fwd) |
intron_variant; nc_transcript_variant |
rs17575556 |
Chr17:44135827(Fwd) |
intron_variant; nc_transcript_variant |
rs17575683 |
Chr17:44139662(Fwd) |
intron_variant; nc_transcript_variant |
rs2838 |
Chr17:44141347(Fwd) |
intron_variant; nc_transcript_variant |
rs17654016 |
Chr17:44137925(Fwd) |
intron_variant; nc_transcript_variant |
rs2316951 |
Chr17:44139083(Fwd) |
intron_variant; nc_transcript_variant |
rs17577094 |
Chr17:44187492(Fwd) |
intron_variant; nc_transcript_variant |
rs9303525 |
Chr17:44187257(Fwd) |
intron_variant; nc_transcript_variant |
rs17660847 |
Chr17:44189373(Fwd) |
intron_variant; nc_transcript_variant |
rs17577159 |
Chr17:44188477(Fwd) |
intron_variant; nc_transcript_variant |
rs17660907 |
Chr17:44191085(Fwd) |
intron_variant; nc_transcript_variant |
rs17660865 |
Chr17:44189408(Fwd) |
intron_variant; nc_transcript_variant |
rs17577313 |
Chr17:44191835(Fwd) |
intron_variant; nc_transcript_variant |
rs17660936 |
Chr17:44191159(Fwd) |
intron_variant; nc_transcript_variant |
rs4630591 |
Chr17:44192568(Fwd) |
intron_variant; nc_transcript_variant |
rs4548919 |
Chr17:44192395(Fwd) |
intron_variant; nc_transcript_variant |
rs17661015 |
Chr17:44192957(Fwd) |
intron_variant; nc_transcript_variant |
rs17577369 |
Chr17:44192923(Fwd) |
intron_variant; nc_transcript_variant |
rs17661045 |
Chr17:44194152(Fwd) |
intron_variant; nc_transcript_variant |
rs17661027 |
Chr17:44193097(Fwd) |
intron_variant; nc_transcript_variant |
rs10514901 |
Chr17:44194735(Fwd) |
intron_variant; nc_transcript_variant |
rs17577447 |
Chr17:44194381(Fwd) |
intron_variant; nc_transcript_variant |
rs17660294 |
Chr17:44167101(Fwd) |
intron_variant; nc_transcript_variant |
rs17660337 |
Chr17:44169605(Fwd) |
intron_variant; nc_transcript_variant |
rs17576631 |
Chr17:44170018(Fwd) |
intron_variant; nc_transcript_variant |
rs17660398 |
Chr17:44170612(Fwd) |
intron_variant; nc_transcript_variant |
rs17576695 |
Chr17:44172327(Fwd) |
intron_variant; nc_transcript_variant |
rs17576709 |
Chr17:44173356(Fwd) |
intron_variant; nc_transcript_variant |
rs17660464 |
Chr17:44177993(Fwd) |
intron_variant; nc_transcript_variant |
rs17576779 |
Chr17:44178272(Fwd) |
intron_variant; nc_transcript_variant |
rs17660488 |
Chr17:44178337(Fwd) |
intron_variant; nc_transcript_variant |
rs17576842 |
Chr17:44179992(Fwd) |
intron_variant; nc_transcript_variant |
rs17576870 |
Chr17:44180442(Fwd) |
intron_variant; nc_transcript_variant |
rs17660595 |
Chr17:44180954(Fwd) |
intron_variant; nc_transcript_variant |
rs17576954 |
Chr17:44181933(Fwd) |
intron_variant; nc_transcript_variant |
rs17576989 |
Chr17:44183616(Fwd) |
intron_variant; nc_transcript_variant |
rs17577024 |
Chr17:44186252(Fwd) |
intron_variant; nc_transcript_variant |
rs17577052 |
Chr17:44186301(Fwd) |
intron_variant; nc_transcript_variant |
rs7687 |
Chr17:44103296(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs16940799 |
Chr17:44102933(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs17574040 |
Chr17:44102865(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs1052594 |
Chr17:44102689(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs1052587 |
Chr17:44102604(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs12150542 |
Chr17:44115730(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs11079729 |
Chr17:44115569(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs41437445 |
Chr17:44116238(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12150090 |
Chr17:44115886(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs17574824 |
Chr17:44115107(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17574796 |
Chr17:44115074(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs8077487 |
Chr17:44115440(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs12185243 |
Chr17:44115351(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs41399444 |
Chr17:44121469(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs41374248 |
Chr17:44120442(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs12150447 |
Chr17:44128125(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7218319 |
Chr17:44126365(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs10514897 |
Chr17:44117397(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs7221390 |
Chr17:44116950(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10514898 |
Chr17:44119636(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs41382552 |
Chr17:44118999(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs17574361 |
Chr17:44108202(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs17652961 |
Chr17:44108355(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs17574425 |
Chr17:44109188(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs1076222 |
Chr17:44109769(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs17652748 |
Chr17:44103616(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs2158257 |
Chr17:44104343(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs17574228 |
Chr17:44104509(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs7350928 |
Chr17:44108100(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs17653193 |
Chr17:44112441(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17653211 |
Chr17:44112638(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17653255 |
Chr17:44112743(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4608377 |
Chr17:44113359(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7350980 |
Chr17:44110271(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4597358 |
Chr17:44110670(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17574604 |
Chr17:44111613(Fwd) |
downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant |
rs17653162 |
Chr17:44111827(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2668691 |
Chr17:44293546(Fwd) |
intron_variant; upstream_gene_variant |
rs2668692 |
Chr17:44293020(Fwd) |
intron_variant; upstream_gene_variant |
rs2668695 |
Chr17:44292126(Fwd) |
downstream_gene_variant; intron_variant |
rs2732605 |
Chr17:44291381(Fwd) |
downstream_gene_variant; intron_variant |
rs2696689 |
Chr17:44297148(Fwd) |
intron_variant; upstream_gene_variant |
rs2732630 |
Chr17:44289150(Fwd) |
downstream_gene_variant; intron_variant |
rs2532417 |
Chr17:44289220(Fwd) |
downstream_gene_variant; intron_variant |
rs2668645 |
Chr17:44288640(Fwd) |
downstream_gene_variant; intron_variant |
rs2732629 |
Chr17:44289101(Fwd) |
downstream_gene_variant; intron_variant |
rs2668665 |
Chr17:44290047(Fwd) |
downstream_gene_variant; intron_variant |
rs2732606 |
Chr17:44291365(Fwd) |
downstream_gene_variant; intron_variant |
rs2732631 |
Chr17:44289232(Fwd) |
downstream_gene_variant; intron_variant |
rs2532416 |
Chr17:44289291(Fwd) |
downstream_gene_variant; intron_variant |
rs2696455 |
Chr17:44283571(Fwd) |
intron_variant |
rs2469933 |
Chr17:44285531(Fwd) |
intron_variant |
rs2732674 |
Chr17:44280697(Fwd) |
intron_variant |
rs2668659 |
Chr17:44281452(Fwd) |
intron_variant |
rs2732628 |
Chr17:44288284(Fwd) |
downstream_gene_variant; intron_variant |
rs2532418 |
Chr17:44288579(Fwd) |
downstream_gene_variant; intron_variant |
rs2668653 |
Chr17:44288156(Fwd) |
downstream_gene_variant; intron_variant |
rs2532419 |
Chr17:44288281(Fwd) |
downstream_gene_variant; intron_variant |
rs2732665 |
Chr17:44277691(Fwd) |
downstream_gene_variant; intron_variant |
rs2532229 |
Chr17:44277265(Fwd) |
downstream_gene_variant; intron_variant |
rs2696446 |
Chr17:44278661(Fwd) |
downstream_gene_variant; intron_variant |
rs2532228 |
Chr17:44277818(Fwd) |
downstream_gene_variant; intron_variant |
rs1358438 |
Chr17:44279760(Fwd) |
intron_variant |
rs17664048 |
Chr17:44278742(Fwd) |
downstream_gene_variant; intron_variant |
rs2732675 |
Chr17:44280188(Fwd) |
intron_variant |
rs1358437 |
Chr17:44279803(Fwd) |
intron_variant |
rs2696438 |
Chr17:44272928(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2732660 |
Chr17:44272679(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1048333 |
Chr17:44273919(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs1048343 |
Chr17:44273889(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs1815 |
Chr17:44276578(Fwd) |
downstream_gene_variant; intron_variant |
rs2696440 |
Chr17:44274560(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs2696443 |
Chr17:44276821(Fwd) |
downstream_gene_variant; intron_variant |
rs1816 |
Chr17:44276618(Fwd) |
downstream_gene_variant; intron_variant |
rs2696709 |
Chr17:44265477(Fwd) |
intron_variant |
rs2732589 |
Chr17:44266022(Fwd) |
intron_variant; upstream_gene_variant |
rs1918788 |
Chr17:44267617(Fwd) |
intron_variant; upstream_gene_variant |
rs2696526 |
Chr17:44267863(Fwd) |
intron_variant; upstream_gene_variant |
rs2732596 |
Chr17:44269546(Fwd) |
intron_variant; upstream_gene_variant |
rs2532235 |
Chr17:44272000(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2532234 |
Chr17:44272266(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17663792 |
Chr17:44272552(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2696701 |
Chr17:44259919(Fwd) |
intron_variant |
rs2696702 |
Chr17:44260416(Fwd) |
intron_variant |
rs2696704 |
Chr17:44261753(Fwd) |
intron_variant |
rs2532246 |
Chr17:44262418(Fwd) |
intron_variant |
rs17663351 |
Chr17:44263923(Fwd) |
intron_variant |
rs2696706 |
Chr17:44264045(Fwd) |
intron_variant |
rs2696707 |
Chr17:44264717(Fwd) |
intron_variant |
rs2696708 |
Chr17:44264943(Fwd) |
intron_variant |
rs12450486 |
Chr17:44264785(Fwd) |
intron_variant |
rs2696577 |
Chr17:44227882(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1918793 |
Chr17:44228169(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17585012 |
Chr17:44227510(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17662115 |
Chr17:44227531(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1918790 |
Chr17:44228619(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2696576 |
Chr17:44228770(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1918792 |
Chr17:44228529(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1918791 |
Chr17:44228609(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532302 |
Chr17:44229415(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2696574 |
Chr17:44230097(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2696575 |
Chr17:44228824(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532303 |
Chr17:44229364(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532297 |
Chr17:44231326(Fwd) |
intron_variant; nc_transcript_variant |
rs2696572 |
Chr17:44231617(Fwd) |
intron_variant; nc_transcript_variant |
rs2696573 |
Chr17:44230647(Fwd) |
intron_variant; nc_transcript_variant |
rs2532298 |
Chr17:44231295(Fwd) |
intron_variant; nc_transcript_variant |
rs1918799 |
Chr17:44218242(Fwd) |
intron_variant; nc_transcript_variant |
rs1918800 |
Chr17:44218138(Fwd) |
intron_variant; nc_transcript_variant |
rs1918801 |
Chr17:44218044(Fwd) |
intron_variant; nc_transcript_variant |
rs2532313 |
Chr17:44217293(Fwd) |
intron_variant; nc_transcript_variant |
rs2696590 |
Chr17:44221602(Fwd) |
intron_variant; nc_transcript_variant |
rs2696592 |
Chr17:44221476(Fwd) |
intron_variant; nc_transcript_variant |
rs2532307 |
Chr17:44221350(Fwd) |
intron_variant; nc_transcript_variant |
rs1528075 |
Chr17:44220454(Fwd) |
intron_variant; nc_transcript_variant |
rs2696587 |
Chr17:44222460(Fwd) |
intron_variant; nc_transcript_variant |
rs1918798 |
Chr17:44222335(Fwd) |
intron_variant; nc_transcript_variant |
rs1406074 |
Chr17:44222067(Fwd) |
intron_variant; nc_transcript_variant |
rs2222746 |
Chr17:44222019(Fwd) |
intron_variant; nc_transcript_variant |
rs2696581 |
Chr17:44227186(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1406069 |
Chr17:44225886(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1918797 |
Chr17:44223243(Fwd) |
intron_variant; nc_transcript_variant |
rs2532305 |
Chr17:44223060(Fwd) |
intron_variant; nc_transcript_variant |
rs17577954 |
Chr17:44209628(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17577975 |
Chr17:44210442(Fwd) |
intron_variant; nc_transcript_variant |
rs7207582 |
Chr17:44210933(Fwd) |
intron_variant; nc_transcript_variant |
rs12150087 |
Chr17:44210988(Fwd) |
intron_variant; nc_transcript_variant |
rs10221243 |
Chr17:44212310(Fwd) |
intron_variant; nc_transcript_variant |
rs9915547 |
Chr17:44212782(Fwd) |
intron_variant; nc_transcript_variant |
rs12150320 |
Chr17:44213204(Fwd) |
intron_variant; nc_transcript_variant |
rs2532316 |
Chr17:44213712(Fwd) |
intron_variant; nc_transcript_variant |
rs2696605 |
Chr17:44213921(Fwd) |
intron_variant; nc_transcript_variant |
rs2532315 |
Chr17:44213934(Fwd) |
intron_variant; nc_transcript_variant |
rs2696604 |
Chr17:44214094(Fwd) |
intron_variant; nc_transcript_variant |
rs2077551 |
Chr17:44214888(Fwd) |
intron_variant; nc_transcript_variant |
rs2696602 |
Chr17:44215896(Fwd) |
intron_variant; nc_transcript_variant |
rs2696601 |
Chr17:44216158(Fwd) |
intron_variant; nc_transcript_variant |
rs2696600 |
Chr17:44216226(Fwd) |
intron_variant; nc_transcript_variant |
rs2532314 |
Chr17:44217112(Fwd) |
intron_variant; nc_transcript_variant |
rs17661141 |
Chr17:44196015(Fwd) |
intron_variant; nc_transcript_variant |
rs17577496 |
Chr17:44194835(Fwd) |
intron_variant; nc_transcript_variant |
rs4383188 |
Chr17:44197603(Fwd) |
intron_variant; nc_transcript_variant |
rs1468241 |
Chr17:44196153(Fwd) |
intron_variant; nc_transcript_variant |
rs4471723 |
Chr17:44205690(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17577650 |
Chr17:44205500(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1122380 |
Chr17:44206079(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1122381 |
Chr17:44205839(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17661348 |
Chr17:44207066(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10514903 |
Chr17:44206646(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10514904 |
Chr17:44207887(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17661385 |
Chr17:44207778(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17577877 |
Chr17:44208218(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17661428 |
Chr17:44208144(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs8070942 |
Chr17:44208674(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs6503457 |
Chr17:44208312(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2696696 |
Chr17:44255777(Fwd) |
intron_variant |
rs2532253 |
Chr17:44256296(Fwd) |
intron_variant |
rs2532256 |
Chr17:44255017(Fwd) |
intron_variant |
rs2532255 |
Chr17:44255532(Fwd) |
intron_variant |
rs2732647 |
Chr17:44254413(Fwd) |
intron_variant; upstream_gene_variant |
rs2532257 |
Chr17:44254494(Fwd) |
intron_variant; upstream_gene_variant |
rs2732645 |
Chr17:44254291(Fwd) |
intron_variant; upstream_gene_variant |
rs2732646 |
Chr17:44254379(Fwd) |
intron_variant; upstream_gene_variant |
rs2732585 |
Chr17:44259539(Fwd) |
intron_variant |
rs2696700 |
Chr17:44259792(Fwd) |
intron_variant |
rs740705 |
Chr17:44258446(Fwd) |
intron_variant |
rs12150012 |
Chr17:44259519(Fwd) |
intron_variant |
rs740706 |
Chr17:44258354(Fwd) |
intron_variant |
rs758523 |
Chr17:44258422(Fwd) |
intron_variant |
rs740708 |
Chr17:44256655(Fwd) |
intron_variant |
rs1881195 |
Chr17:44257473(Fwd) |
intron_variant |
rs2532270 |
Chr17:44249800(Fwd) |
intron_variant; upstream_gene_variant |
rs2696662 |
Chr17:44249621(Fwd) |
intron_variant; upstream_gene_variant |
rs17585974 |
Chr17:44249199(Fwd) |
5_prime_UTR_variant; downstream_gene_variant; missense_variant; upstream_gene_variant |
rs17662889 |
Chr17:44249096(Fwd) |
5_prime_UTR_variant; downstream_gene_variant; synonymous_variant; upstream_gene_variant |
rs1881194 |
Chr17:44248814(Fwd) |
5_prime_UTR_variant; downstream_gene_variant; synonymous_variant; upstream_gene_variant |
rs1881193 |
Chr17:44248769(Fwd) |
5_prime_UTR_variant; downstream_gene_variant; missense_variant; synonymous_variant; upstream_gene_variant |
rs2532271 |
Chr17:44248042(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532273 |
Chr17:44247314(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532259 |
Chr17:44253364(Fwd) |
intron_variant; upstream_gene_variant |
rs2532264 |
Chr17:44252416(Fwd) |
intron_variant; upstream_gene_variant |
rs2696666 |
Chr17:44251972(Fwd) |
intron_variant; upstream_gene_variant |
rs2732643 |
Chr17:44251907(Fwd) |
intron_variant; upstream_gene_variant |
rs956329 |
Chr17:44251230(Fwd) |
intron_variant; upstream_gene_variant |
rs2532267 |
Chr17:44250616(Fwd) |
intron_variant; upstream_gene_variant |
rs2532268 |
Chr17:44250473(Fwd) |
intron_variant; upstream_gene_variant |
rs2532269 |
Chr17:44250108(Fwd) |
intron_variant; upstream_gene_variant |
rs17585608 |
Chr17:44243979(Fwd) |
intron_variant; nc_transcript_variant |
rs2696684 |
Chr17:44244397(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17585644 |
Chr17:44244581(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532282 |
Chr17:44244896(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2141299 |
Chr17:44240986(Fwd) |
intron_variant; nc_transcript_variant |
rs2696567 |
Chr17:44241304(Fwd) |
intron_variant; nc_transcript_variant |
rs2532286 |
Chr17:44241664(Fwd) |
intron_variant; nc_transcript_variant |
rs4792843 |
Chr17:44243179(Fwd) |
intron_variant; nc_transcript_variant |
rs2532278 |
Chr17:44246405(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532277 |
Chr17:44246527(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532276 |
Chr17:44246624(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532275 |
Chr17:44246997(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2696657 |
Chr17:44244926(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532281 |
Chr17:44245171(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2532280 |
Chr17:44245359(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2696660 |
Chr17:44246211(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1528074 |
Chr17:44234060(Fwd) |
intron_variant; nc_transcript_variant |
rs17585214 |
Chr17:44233811(Fwd) |
intron_variant; nc_transcript_variant |
rs1528072 |
Chr17:44236725(Fwd) |
intron_variant; nc_transcript_variant |
rs1406068 |
Chr17:44234526(Fwd) |
intron_variant; nc_transcript_variant |
rs2109092 |
Chr17:44232959(Fwd) |
intron_variant; nc_transcript_variant |
rs2532296 |
Chr17:44231827(Fwd) |
intron_variant; nc_transcript_variant |
rs17662235 |
Chr17:44233776(Fwd) |
intron_variant; nc_transcript_variant |
rs1534456 |
Chr17:44232990(Fwd) |
intron_variant; nc_transcript_variant |
rs17585426 |
Chr17:44238966(Fwd) |
intron_variant; nc_transcript_variant |
rs17662403 |
Chr17:44238938(Fwd) |
intron_variant; nc_transcript_variant |
rs1918789 |
Chr17:44240107(Fwd) |
intron_variant; nc_transcript_variant |
rs2532288 |
Chr17:44239958(Fwd) |
intron_variant; nc_transcript_variant |
rs2696571 |
Chr17:44237372(Fwd) |
intron_variant; nc_transcript_variant |
rs2532292 |
Chr17:44237068(Fwd) |
intron_variant; nc_transcript_variant |
rs2532290 |
Chr17:44238490(Fwd) |
intron_variant; nc_transcript_variant |
rs2532291 |
Chr17:44238424(Fwd) |
intron_variant; nc_transcript_variant |