Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 8
rs2853969 1.000 6 31388797 regulatory region variant G/A snv 0.10 2