Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1042636 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1801726 0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs756322971 0.763 0.240 3 122284955 missense variant C/A;G snv 9
rs11746443 0.882 0.120 5 177371305 intron variant G/A snv 0.24 0.21 4
rs1042138 0.882 0.120 7 93426338 3 prime UTR variant G/A snv 0.15 0.11 3
rs4236480 0.882 0.120 7 142929454 missense variant T/A;C;G snv 3