Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 3
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs2328223 20 17865277 intergenic variant A/C;G;T snv 2
rs10249276 7 118938630 intergenic variant A/G;T snv 1
rs10281955 7 118944637 intergenic variant G/A snv 0.86 1
rs10433415 3 133566686 intergenic variant G/T snv 0.57 1
rs10935068 3 133543963 upstream gene variant T/A;G snv 1
rs10953881 7 118968071 intergenic variant C/G;T snv 1
rs10953885 7 118968349 intergenic variant T/A;C snv 1
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 1
rs11128951 3 20334054 intron variant A/G snv 0.19 1
rs12108602 4 114719413 upstream gene variant A/G snv 0.18 1
rs13149993 4 80237391 regulatory region variant G/A;C snv 1
rs13209747 6 126794309 intron variant C/G;T snv 0.36 1
rs1444600 3 133569662 upstream gene variant C/T snv 0.57 1
rs170099 7 119360158 intergenic variant C/T snv 0.84 1
rs17144687 5 118824240 intergenic variant A/C snv 4.5E-02 1
rs2677485 2 155678644 intergenic variant T/A;C snv 1
rs2749097 1 63661797 downstream gene variant C/G snv 0.19 1
rs35444 12 115114632 intergenic variant A/G snv 0.38 1