Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10101385 8 118911611 regulatory region variant A/G snv 0.34 1
rs1021188 13 42541997 intergenic variant C/T snv 0.79 1
rs10242100 7 121343289 downstream gene variant A/G snv 0.29 1
rs10493013 1 22376542 regulatory region variant T/C snv 0.20 1
rs10502386 18 8966146 intergenic variant G/T snv 0.39 1
rs10835187 11 27484130 downstream gene variant C/T snv 0.41 1
rs10872676 6 151622842 downstream gene variant C/A;T snv 1
rs11755164 6 44671447 regulatory region variant T/C snv 0.57 1
rs11803476 1 22376832 regulatory region variant C/T snv 0.15 1
rs11810369 1 22361158 downstream gene variant G/A snv 0.22 1
rs11972702 7 38108059 regulatory region variant C/A;T snv 1
rs12197785 6 151639470 intergenic variant C/G;T snv 1
rs12561997 1 22375787 TF binding site variant G/A snv 0.15 1
rs12723796 1 22365113 non coding transcript exon variant G/A snv 0.16 1
rs12742784 1.000 0.080 1 22355873 intergenic variant C/A;T snv 1
rs12750721 1 22362780 downstream gene variant G/A snv 0.22 1
rs12756978 1 22358262 intergenic variant G/C snv 0.20 1
rs12821008 12 49080822 intergenic variant C/T snv 0.30 1
rs12861586 13 42336328 upstream gene variant C/A;T snv 1
rs12932673 16 86676125 regulatory region variant C/G;T snv 0.16 1
rs13204965 6 126845927 intron variant A/C;T snv 1
rs13277230 8 118910754 downstream gene variant C/T snv 0.34 1
rs13439134 8 118906629 downstream gene variant G/C snv 0.34 1
rs1346004 2 165744536 downstream gene variant G/A;T snv 1
rs1357651 7 38058260 intergenic variant T/G snv 0.64 1