Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs861530 0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs1805329 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 15
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147