Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5751129 0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs74911261 0.882 0.160 11 108486410 missense variant G/A snv 1.6E-02 1.6E-02 4
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58