Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10990303 9 95648123 upstream gene variant C/G;T snv 1
rs11741704 5 8116712 intergenic variant T/A;C;G snv 1
rs11913445 22 20154990 upstream gene variant C/A;T snv 1
rs13188458 0.882 0.160 5 8127718 intergenic variant T/G snv 0.22 1
rs13192994 6 75529546 intergenic variant A/C snv 0.10 1
rs1423056 19 33289538 upstream gene variant G/A snv 0.24 1
rs1465370 7 130373797 TF binding site variant G/T snv 0.38 1
rs1555091 6 127115500 intron variant G/A snv 0.30 1
rs1594477 17 70511295 intergenic variant T/A;C snv 1
rs167025 5 74137483 intron variant G/A snv 0.28 1
rs16848284 4 72611184 intergenic variant T/C snv 0.39 1
rs17033702 2 67516476 intergenic variant C/G;T snv 1
rs173269 17 70512851 intergenic variant G/A snv 0.25 1
rs2580821 2 231939445 intergenic variant C/A snv 6.6E-02 1
rs2696625 17 46249498 downstream gene variant A/G snv 0.15 1
rs2943658 2 226258868 intergenic variant A/G;T snv 1
rs2988004 9 37044391 upstream gene variant T/C;G snv 1
rs3094622 6 30360175 upstream gene variant A/G snv 8.4E-02 1
rs4650943 1 176445645 intron variant A/G snv 0.46 1
rs4865656 5 51363954 intergenic variant G/A snv 0.45 1
rs59499656 18 43188344 intergenic variant A/T snv 0.43 1
rs6107848 20 6610469 intergenic variant A/G snv 0.62 1
rs6689056 1 24038041 upstream gene variant G/A;C snv 1
rs6766897 3 134472461 regulatory region variant C/A snv 0.65 1
rs6870096 5 152566250 intron variant C/G snv 0.70 1