Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs1161457931 0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs2234671 0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs57749775 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs143175221 0.827 0.200 6 26092952 missense variant T/C snv 8.4E-04 5.6E-04 5
rs121918664 0.851 0.120 5 1254395 missense variant C/T snv 5.2E-05 9.1E-05 4