Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4938303 11 116714271 intergenic variant C/A;T snv 0.62 5
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs12708967 16 56959299 upstream gene variant T/C snv 0.18 4
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs17410914 8 19985951 intergenic variant C/A;T snv 4
rs17411126 8 19997761 intergenic variant T/C snv 0.26 4
rs17489268 8 19994534 regulatory region variant T/A snv 0.25 4
rs17489282 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 4
rs1919484 1.000 0.040 8 20012165 intergenic variant G/A snv 0.23 4
rs1936800 6 127114919 intron variant C/T snv 0.51 4
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 4
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs2954031 8 125479491 intron variant G/T snv 0.42 4
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 4
rs4871603 8 125468125 intron variant C/T snv 0.59 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs7811025 7 99788078 upstream gene variant C/T snv 4.8E-02 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3