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
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
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs3213245 0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13