#rs
|
Location
|
Annotation
|
No. of Studies (Positive/Negative)
|
| rs6265 |
chr11:27679916(Forward) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant |
7(5/2) |
| rs2230912 |
chr12:121622196(Forward) |
3_prime_UTR_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
6(3/3) |
| rs242939 |
chr17:43895579(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
3(3/0) |
| rs4680 |
chr22:19951271(Forward) |
downstream_gene_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
3(2/1) |
| rs2522833 |
chr7:82453708(Forward) |
missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
3(3/0) |
| rs11030101 |
chr11:27680744(Forward) |
5_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
2(1/1) |
| rs40184 |
chr5:1395077(Forward) |
intron_variant |
2(1/1) |
| rs1006737 |
chr12:2345295(Forward) |
intron_variant |
2(2/0) |
| rs1137070 |
chrX:43603391(Forward) |
nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
2(2/0) |
| rs6311 |
chr13:47471478(Forward) |
upstream_gene_variant |
2(1/1) |
| rs1545843 |
chr12:84564068(Forward) |
|
2(2/0) |
| rs2072446 |
chr17:47587819(Forward) |
downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant |
2(2/0) |
| rs2242446 |
chr16:55690425(Forward) |
5_prime_UTR_variant; intron_variant; upstream_gene_variant |
2(2/0) |
| rs9340799 |
chr6:152163381(Forward) |
intron_variant |
2(2/0) |
| rs110402 |
chr17:43880047(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
2(2/0) |
| rs2715148 |
chr7:82450035(Forward) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
2(2/0) |
| rs3794996 |
chr19:19754942(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs7013994 |
chr8:58226060(Forward) |
|
1(0/1) |
| rs701865 |
chr10:95381773(Forward) |
missense_variant |
1(1/0) |
| rs8122984 |
chr20:58352921(Forward) |
intron_variant |
1(0/1) |
| rs17226852 |
chr20:13973760(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs1513105 |
chr12:71098168(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(1/0) |
| rs7490744 |
chr13:84976969(Forward) |
|
1(0/1) |
| rs2268666 |
chr6:146746088(Forward) |
intron_variant |
1(1/0) |
| rs6781822 |
chr3:11675632(Forward) |
intron_variant; NMD_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs3745406 |
chr19:54394965(Forward) |
downstream_gene_variant; synonymous_variant |
1(1/0) |
| rs7551221 |
chr1:162000398(Forward) |
|
1(0/1) |
| rs7676614 |
chr4:144616366(Forward) |
intron_variant |
1(0/1) |
| rs6465084 |
chr7:86403475(Forward) |
downstream_gene_variant; intron_variant |
1(1/0) |
| rs12273539 |
chr11:27683311(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs880090 |
chr19:19740729(Forward) |
3_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs1049353 |
chr6:88853635(Forward) |
3_prime_UTR_variant; downstream_gene_variant; synonymous_variant |
1(1/0) |
| rs850815 |
chr15:23894745(Forward) |
upstream_gene_variant |
1(0/1) |
| rs1843809 |
chr12:72348698(Forward) |
intron_variant; NMD_transcript_variant |
1(1/0) |
| rs2234693 |
chr6:152163335(Forward) |
intron_variant |
1(1/0) |
| rs2433320 |
chr4:95370805(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs882632 |
chr2:29280761(Forward) |
downstream_gene_variant |
1(0/1) |
| rs6191 |
chr5:142658156(Forward) |
3_prime_UTR_variant; downstream_gene_variant |
1(1/0) |
| rs9943849 |
chr12:69370756(Forward) |
|
1(1/0) |
| rs1045642 |
chr7:87138645(Forward) |
3_prime_UTR_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant |
1(1/0) |
| rs1344677 |
chr12:105050967(Forward) |
intron_variant |
1(0/1) |
| rs270545 |
chr5:38051593(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs7566637 |
chr2:10422939(Forward) |
downstream_gene_variant |
1(0/1) |
| rs2073380 |
chr21:47863757(Forward) |
downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
1(1/0) |
| rs676389 |
chr6:165912970(Forward) |
intron_variant |
1(1/0) |
| rs4709845 |
chr6:164900598(Forward) |
|
1(1/0) |
| rs2384061 |
chr2:25135620(Forward) |
intron_variant |
1(0/1) |
| rs11764174 |
chr7:12596616(Forward) |
|
1(0/1) |
| rs7318876 |
chr13:46179227(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs1143643 |
chr2:113588302(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(1/0) |
| rs5916245 |
chrX:5661536(Forward) |
|
1(0/1) |
| rs8920 |
chr15:23888891(Forward) |
3_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant |
1(0/1) |
| rs7103873 |
chr11:27700317(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(0/1) |
| rs7242 |
chr7:100781445(Forward) |
3_prime_UTR_variant |
1(1/0) |
| rs1430306 |
chr2:109807885(Forward) |
intron_variant |
1(0/1) |
| rs1057910 |
chr10:96741053(Forward) |
missense_variant |
1(1/0) |
| rs1676089 |
chr18:49194509(Forward) |
|
1(0/1) |
| rs13130123 |
chr4:144508588(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs826824 |
chr7:147058991(Forward) |
intron_variant |
1(0/1) |
| rs10815615 |
chr9:7485343(Forward) |
|
1(0/1) |
| rs9538386 |
chr13:59896050(Forward) |
|
1(0/1) |
| rs9939609 |
chr16:53820527(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(1/0) |
| rs2464805 |
chr5:112101793(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(1/0) |
| rs2898938 |
chr11:3832257(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs1360780 |
chr6:35607571(Forward) |
intron_variant |
1(1/0) |
| rs13340364 |
chr5:102339110(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs2227684 |
chr7:100776931(Forward) |
downstream_gene_variant; intron_variant |
1(1/0) |
| rs2043293 |
chr19:19751456(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs17144465 |
chr7:21504427(Forward) |
intron_variant; NMD_transcript_variant |
1(0/1) |
| rs10989591 |
chr9:104449098(Forward) |
missense_variant |
1(1/0) |
| rs3788265 |
chr21:47833789(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs867640 |
chr17:61601945(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
1(1/0) |
| rs2240403 |
chr7:30695202(Forward) |
3_prime_UTR_variant; NMD_transcript_variant; synonymous_variant |
1(1/0) |
| rs5522 |
chr4:149357475(Forward) |
missense_variant |
1(1/0) |
| rs590557 |
chr2:31461395(Forward) |
intron_variant; upstream_gene_variant |
1(0/1) |
| rs1112714 |
chr4:144503647(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs1167264 |
chr1:49933045(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs8191992 |
chr7:136701308(Forward) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
1(1/0) |
| rs766288 |
chr1:231693688(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs2702199 |
chr1:183401880(Forward) |
|
1(0/1) |
| rs10835210 |
chr11:27695910(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(0/1) |
| rs715217 |
chr20:1472408(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(0/1) |
| rs6280 |
chr3:113890815(Forward) |
missense_variant |
1(1/0) |
| rs1202184 |
chr7:87213901(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
1(1/0) |
| rs1526285 |
chr2:150508525(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs6686529 |
chr1:215410106(Forward) |
3_prime_UTR_variant; downstream_gene_variant |
1(1/0) |
| rs3775845 |
chr4:120432447(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs6589849 |
chr11:98886331(Forward) |
|
1(1/0) |
| rs6313 |
chr13:47469940(Forward) |
intron_variant; synonymous_variant |
1(1/0) |
| rs2710102 |
chr7:147574390(Forward) |
intron_variant |
1(1/0) |
| rs28722151 |
chr11:27681176(Forward) |
5_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
1(1/0) |
| rs644926 |
chr2:31489727(Forward) |
3_prime_UTR_variant |
1(1/0) |
| rs11206244 |
chr1:54375701(Forward) |
3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant |
1(1/0) |
| rs2831649 |
chr21:29582347(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(0/1) |
| rs1046248 |
chr14:96703484(Forward) |
5_prime_UTR_variant; missense_variant; upstream_gene_variant |
1(1/0) |
| rs2239307 |
chr16:4042449(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs13074924 |
chr3:174029045(Forward) |
|
1(1/0) |
| rs3748989 |
chr2:1946968(Forward) |
synonymous_variant |
1(1/0) |
| rs2631522 |
chr16:55225083(Forward) |
|
1(0/1) |
| rs4941807 |
chr13:35525949(Forward) |
intron_variant |
1(1/0) |
| rs12651937 |
chr5:77922539(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs650058 |
chr10:95378547(Forward) |
intron_variant |
1(1/0) |
| rs6438552 |
chr3:119631814(Forward) |
intron_variant |
1(1/0) |
| rs11918585 |
chr3:61428182(Forward) |
|
1(0/1) |
| rs2124147 |
chr3:171395468(Forward) |
missense_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant |
1(1/0) |
| rs12278579 |
chr11:42737996(Forward) |
|
1(0/1) |
| rs6945001 |
chr7:26128382(Forward) |
|
1(0/1) |
| rs2213172 |
chr22:23579510(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs1801206 |
chr4:6302707(Forward) |
downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
1(1/0) |
| rs76481776 |
chr7:129410227(Forward) |
downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
1(1/0) |
| rs1800629 |
chr6:31543031(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs2800092 |
chr10:36613554(Forward) |
|
1(0/1) |
| rs8099455 |
chr18:59261173(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs7127866 |
chr11:82809600(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs4550218 |
chr11:22863658(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(0/1) |
| rs2070744 |
chr7:150690079(Forward) |
intron_variant; upstream_gene_variant |
1(0/1) |
| rs3761418 |
chr22:23521094(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs2267013 |
chr22:23545879(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs7797729 |
chr7:129310092(Forward) |
intron_variant |
1(0/1) |
| rs1922242 |
chr7:87173667(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
1(1/0) |
| rs4238989 |
chr17:74463388(Forward) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
1(1/0) |
| rs11030103 |
chr11:27682333(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs1653765 |
chr2:23729232(Forward) |
downstream_gene_variant; intron_variant |
1(0/1) |
| rs606149 |
chr1:193921548(Forward) |
|
1(1/0) |
| rs805284 |
chr6:31682029(Forward) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
1(0/1) |
| rs7942744 |
chr11:6743890(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs10997875 |
chr10:69679824(Forward) |
downstream_gene_variant |
1(1/0) |
| rs6198 |
chr5:142657621(Forward) |
3_prime_UTR_variant; downstream_gene_variant |
1(1/0) |
| rs1024611 |
chr17:32579788(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs17110747 |
chr12:72425954(Forward) |
3_prime_UTR_variant; intron_variant; nc_transcript_variant |
1(1/0) |
| rs619002 |
chr2:31488965(Forward) |
intron_variant |
1(1/0) |
| rs11123857 |
chr2:101603812(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
1(1/0) |
| rs7596956 |
chr2:220152359(Forward) |
downstream_gene_variant |
1(0/1) |
| rs4311 |
chr17:61560763(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs2770248 |
chr13:112017894(Forward) |
|
1(1/0) |
| rs1386494 |
chr12:72352543(Forward) |
intron_variant; NMD_transcript_variant |
1(1/0) |
| rs7728378 |
chr5:76259350(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(1/0) |
| rs11231662 |
chr11:63738642(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(0/1) |
| rs6813541 |
chr4:174772568(Forward) |
|
1(0/1) |
| rs9564791 |
chr13:71798043(Forward) |
|
1(0/1) |
| rs3770018 |
chr2:178540804(Forward) |
intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
1(1/0) |
| rs627419 |
chr18:66315758(Forward) |
|
1(0/1) |
| rs9311395 |
chr3:4741821(Forward) |
intron_variant |
1(0/1) |
| rs41282918 |
chr11:27678780(Forward) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant |
1(1/0) |
| rs3794764 |
chr17:26111428(Forward) |
intron_variant |
1(1/0) |
| rs12923267 |
chr16:65538017(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs9394026 |
chr6:30982544(Forward) |
intron_variant |
1(0/1) |
| rs7012271 |
chr8:114317672(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(0/1) |
| rs242924 |
chr17:43885367(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(1/0) |
| rs10835065 |
chr11:26772618(Forward) |
|
1(0/1) |
| rs1786330 |
chr8:101692130(Forward) |
upstream_gene_variant |
1(0/1) |
| rs2276307 |
chr11:113803887(Forward) |
intron_variant |
1(1/0) |
| rs310501 |
chr5:82889910(Forward) |
|
1(1/0) |
| rs3777514 |
chr6:90020581(Forward) |
intron_variant |
1(1/0) |
| rs11024034 |
chr11:2790163(Forward) |
intron_variant; upstream_gene_variant |
1(0/1) |
| rs2271933 |
chr1:32092525(Forward) |
downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant |
1(1/0) |
| rs4238010 |
chr12:4118317(Forward) |
|
1(0/1) |
| rs1517057 |
chr3:166444013(Forward) |
downstream_gene_variant |
1(0/1) |
| rs8003655 |
chr14:86197347(Forward) |
|
1(0/1) |
| rs7718461 |
chr5:76258048(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs17657363 |
chr1:171801416(Forward) |
|
1(0/1) |
| rs4295 |
chr17:61556298(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(1/0) |
| rs17077540 |
chr18:65285279(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs11039588 |
chr11:48234357(Forward) |
upstream_gene_variant |
1(1/0) |
| rs16147 |
chr7:24323410(Forward) |
upstream_gene_variant |
1(1/0) |
| rs472952 |
chr1:66800764(Forward) |
downstream_gene_variant; intron_variant |
1(1/0) |
| rs2276308 |
chr11:113803976(Forward) |
intron_variant |
1(1/0) |
| rs2287161 |
chr12:107381140(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs4131347 |
chr12:72324371(Forward) |
downstream_gene_variant |
1(0/1) |
| rs709496 |
chr3:107697427(Forward) |
|
1(0/1) |
| rs9352774 |
chr6:64014812(Forward) |
intron_variant; NMD_transcript_variant |
1(1/0) |
| rs6136667 |
chr20:1978301(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs2284220 |
chr7:30718103(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
1(1/0) |
| rs11569126 |
chr4:110929653(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs2616976 |
chr8:4478239(Forward) |
intron_variant |
1(0/1) |
| rs625588 |
chr2:224602647(Forward) |
|
1(0/1) |
| rs1799983 |
chr7:150696111(Forward) |
intron_variant; missense_variant; upstream_gene_variant |
1(0/1) |
| rs3810950 |
chr10:50824619(Forward) |
downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
1(1/0) |
| rs3806318 |
chr1:65885357(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs12125058 |
chr1:221277508(Forward) |
|
1(0/1) |
| rs13013430 |
chr2:75414997(Forward) |
intron_variant |
1(1/0) |
| rs948854 |
chr11:68450203(Forward) |
upstream_gene_variant |
1(1/0) |
| rs3779250 |
chr7:30694260(Forward) |
intron_variant; NMD_transcript_variant |
1(1/0) |
| rs12049330 |
chr1:110031188(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs4478239 |
chr4:188191306(Forward) |
|
1(0/1) |
| rs878567 |
chr5:63255991(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(1/0) |
| rs10833965 |
chr11:23214880(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs11568817 |
chr6:78173382(Forward) |
5_prime_UTR_variant |
1(1/0) |
| rs12692709 |
chr2:164894561(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs821616 |
chr1:232144598(Forward) |
3_prime_UTR_variant; missense_variant |
1(1/0) |
| rs17299191 |
chr16:55472083(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs4537731 |
chr11:18068882(Forward) |
upstream_gene_variant |
1(1/0) |
| rs17400379 |
chr7:94209932(Forward) |
downstream_gene_variant |
1(0/1) |
| rs976576 |
chr5:32722499(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs27520 |
chr5:11218488(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(0/1) |
| rs1430871 |
chr11:103145170(Forward) |
intron_variant |
1(0/1) |
| rs9572423 |
chr13:70846203(Forward) |
|
1(0/1) |
| rs17105696 |
chr14:37387827(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs1313925 |
chr4:103377576(Forward) |
upstream_gene_variant |
1(0/1) |
| rs4760933 |
chr12:71143758(Forward) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
1(0/1) |
| rs6318 |
chrX:113965735(Forward) |
missense_variant |
1(1/0) |
| rs3760138 |
chr17:74463109(Forward) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
1(1/0) |
| rs6537837 |
chr1:110119732(Forward) |
intron_variant |
1(0/1) |
| rs2692359 |
chr7:145807447(Forward) |
|
1(1/0) |
| rs563556 |
chr5:112153996(Forward) |
intron_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs885479 |
chr16:89986154(Forward) |
downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
1(1/0) |
| rs2638463 |
chr12:89669785(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs695884 |
chr3:191148080(Forward) |
|
1(0/1) |
| rs5443 |
chr12:6954875(Forward) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
1(1/0) |
| rs7713917 |
chr5:78829249(Forward) |
downstream_gene_variant; upstream_gene_variant |
1(1/0) |
| rs1801133 |
chr1:11856378(Forward) |
downstream_gene_variant; missense_variant |
1(1/0) |
| rs1539243 |
chr1:206647787(Forward) |
5_prime_UTR_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
1(1/0) |
| rs12520799 |
chr5:134782450(Forward) |
3_prime_UTR_variant; stop_gained; upstream_gene_variant |
1(1/0) |
| rs684302 |
chr11:18060353(Forward) |
intron_variant; NMD_transcript_variant |
1(1/0) |
| rs10514718 |
chr3:61413814(Forward) |
|
1(0/1) |
| rs2352834 |
chr1:147365020(Forward) |
|
1(0/1) |
| rs12581840 |
chr12:19834151(Forward) |
intron_variant |
1(0/1) |
| rs182358 |
chr1:97463150(Forward) |
|
1(0/1) |
| rs2073376 |
chr21:47851753(Forward) |
missense_variant; nc_transcript_variant; non_coding_exon_variant |
1(1/0) |
| rs717602 |
chr6:165807107(Forward) |
intron_variant |
1(1/0) |
| rs4480754 |
chr15:23886941(Forward) |
downstream_gene_variant |
1(0/1) |
| rs2156921 |
chr22:23569063(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs10946320 |
chr6:19461554(Forward) |
|
1(0/1) |
| rs1536723 |
chr13:23798431(Forward) |
intron_variant |
1(0/1) |
| rs16944 |
chr2:113594867(Forward) |
upstream_gene_variant |
1(1/0) |
| rs7333412 |
chr13:47403360(Forward) |
downstream_gene_variant |
1(1/0) |
| rs2828520 |
chr21:25143119(Forward) |
|
1(0/1) |
| rs1386486 |
chr12:72412220(Forward) |
intron_variant |
1(1/0) |
| rs1801262 |
chr2:182543455(Forward) |
intron_variant; missense_variant; nc_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs1800532 |
chr11:18047816(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs2030324 |
chr11:27726915(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(0/1) |
| rs4305 |
chr17:61558229(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs1875999 |
chr5:76264982(Forward) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
1(1/0) |
| rs12633494 |
chr3:61145050(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs112439044 |
chr1:41220077(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
1(1/0) |
| rs2844043 |
chr8:101488821(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs934036 |
chr2:218869388(Forward) |
upstream_gene_variant |
1(0/1) |
| rs6832167 |
chr4:70474310(Forward) |
intron_variant; upstream_gene_variant |
1(0/1) |
| rs493474 |
chr1:199360977(Forward) |
downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
1(0/1) |
| rs16139 |
chr7:24324879(Forward) |
missense_variant |
1(1/0) |
| rs1221754 |
chr2:154372766(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs1064448 |
chr16:50350883(Forward) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant |
1(1/0) |
| rs10447760 |
chr7:113723265(Forward) |
upstream_gene_variant |
1(1/0) |
| rs231779 |
chr2:204734487(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs11569017 |
chr4:110902111(Forward) |
downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
1(1/0) |
| rs5569 |
chr16:55731835(Forward) |
downstream_gene_variant; synonymous_variant; upstream_gene_variant |
1(0/1) |
| rs2171363 |
chr12:72360264(Forward) |
downstream_gene_variant; intron_variant |
1(1/0) |
| rs2304129 |
chr19:19746214(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(1/0) |
| rs4461142 |
chr17:61578048(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
1(1/0) |
| rs6782799 |
chr3:119610793(Forward) |
intron_variant |
1(1/0) |
| rs2253168 |
chr14:69050465(Forward) |
intron_variant; nc_transcript_variant |
1(0/1) |
| rs11254981 |
chr10:7108780(Forward) |
|
1(0/1) |
| rs929122 |
chr6:117605749(Forward) |
downstream_gene_variant |
1(0/1) |
| rs13027103 |
chr2:31891571(Forward) |
|
1(0/1) |
| rs1762444 |
chr10:131250665(Forward) |
|
1(0/1) |
| rs4333 |
chr17:61564522(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs2710117 |
chr7:147601772(Forward) |
intron_variant |
1(1/0) |
| rs2267015 |
chr22:23558561(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs6541281 |
chr1:231813134(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs11938628 |
chr4:115458168(Forward) |
|
1(0/1) |
| rs725308 |
chrX:112830778(Forward) |
|
1(0/1) |
| rs1800866 |
chr9:34637690(Forward) |
5_prime_UTR_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
1(1/0) |
| rs2116624 |
chr7:13404664(Forward) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
1(0/1) |
| rs1176744 |
chr11:113803028(Forward) |
missense_variant |
1(1/0) |
| rs12462886 |
chr19:29263690(Forward) |
|
1(0/1) |
| rs4329 |
chr17:61563458(Forward) |
downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs2031616 |
chr10:94736967(Forward) |
intron_variant; NMD_transcript_variant |
1(0/1) |
| rs4309 |
chr17:61559923(Forward) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant |
1(1/0) |
| rs208294 |
chr12:121600253(Forward) |
3_prime_UTR_variant; 5_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant |
1(0/1) |
| rs220818 |
chr6:165850104(Forward) |
intron_variant |
1(1/0) |
| rs3732293 |
chr2:74649934(Forward) |
downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
1(0/1) |
| rs33388 |
chr5:142697295(Forward) |
intron_variant; nc_transcript_variant |
1(1/0) |
| rs2267012 |
chr22:23535982(Forward) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
1(1/0) |
| rs17767562 |
chr13:97275932(Forward) |
intron_variant |
1(0/1) |
