Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3860498 3 133541672 downstream gene variant T/A;C snv 1
rs4017074 3 133541583 downstream gene variant T/C snv 0.71 1
rs4268066 7 118961051 intergenic variant C/T snv 0.86 1
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 1
rs4518581 7 118970601 intergenic variant G/A snv 0.86 1
rs4730908 7 119017956 intergenic variant C/G;T snv 1
rs4767293 12 112025492 downstream gene variant A/G snv 0.53 1
rs4854723 3 133535414 regulatory region variant A/C snv 0.52 1
rs4854727 3 133539041 downstream gene variant A/G snv 0.65 1
rs4854733 3 133568221 intergenic variant A/G;T snv 1
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 1
rs6073958 20 45923216 downstream gene variant T/C snv 0.22 1
rs6466686 7 118996763 intergenic variant C/T snv 0.58 1
rs6763627 3 133543723 upstream gene variant C/G;T snv 1
rs6778062 3 133548309 upstream gene variant G/C snv 0.66 1
rs6785365 3 133543601 upstream gene variant A/G snv 0.65 1
rs7614812 3 133545407 upstream gene variant C/A snv 0.62 1
rs7812233 7 118978108 intergenic variant G/A snv 0.86 1
rs855350 1 63661333 downstream gene variant C/T snv 0.43 1
rs871606 4 53933078 intron variant T/C;G snv 1
rs872134 3 133546688 upstream gene variant G/T snv 0.57 1
rs9292468 5 32818967 intergenic variant T/A;C snv 1
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 4
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6