Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs80356616 0.732 0.360 11 17387917 missense variant C/T snv 19
rs80356624 0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs1050828 0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs121909244 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs137853240 0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs80356618 0.807 0.200 11 17387595 missense variant C/A;T snv 8
rs572115942 0.925 0.240 16 30756714 missense variant G/A snv 8.0E-05 7.7E-05 7
rs137853238 0.807 0.200 12 120994265 missense variant G/A snv 6
rs267607555 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs1272388614 0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5
rs146488435 0.851 0.080 17 63533914 missense variant C/G;T snv 8.0E-06; 6.4E-05 5