Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6