Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs2023239 0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2494732 0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs2295633 0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs806374 0.925 0.080 6 88147601 intron variant T/C snv 0.37 2