Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs211037 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs686 0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs878853161 0.851 0.240 1 42929977 frameshift variant AT/- del 7
rs1131692040 0.882 0.160 X 154399844 missense variant A/G snv 4