Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs179008 0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs2227513 1.000 0.080 12 68253559 intron variant T/C snv 0.15 3