Disease: Alcohol consumption
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs7570971
RAB3GAP1
1.000 0.080 2 135080336 intron variant C/A snv 0.61 5