Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs174538 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs13042395 0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 13
rs1800477 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs2236142 0.827 0.120 22 28741956 5 prime UTR variant G/C snv 0.66 6
rs6720283 0.882 0.120 2 237401239 intron variant G/A snv 0.31 4
rs738722 0.882 0.120 22 28734024 intron variant T/C snv 0.67 4