Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2179367 0.925 0.120 6 149441401 regulatory region variant A/G snv 0.50 1
rs7838717
BOP1
1.000 0.120 8 144280310 intron variant C/T snv 0.30 3
rs7071275 1.000 0.120 10 121662920 regulatory region variant C/T snv 0.19 1
rs10809650 0.925 0.120 9 1202371 intergenic variant A/G snv 0.26 1
rs12342106 1.000 0.120 9 1201156 regulatory region variant G/A snv 0.32 1
rs4730775
WNT2
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41 1
rs38904 1.000 0.120 7 117252792 intergenic variant T/C snv 0.52 2
rs611744
EIF3E
0.925 0.120 8 108215779 intron variant A/G;T snv 1