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
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1076560 0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs686 0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs2235749 0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs1042114 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs2234918 0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs751416416 0.882 0.120 8 53250920 missense variant C/A;T snv 8.3E-06; 4.1E-06 5
rs910080 0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35 4
rs2236861 0.882 0.080 1 28813244 intron variant G/A snv 0.19 3
rs1022563 0.925 0.080 20 1973693 intron variant C/G;T snv 2