Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
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
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
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
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
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
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs75961395 0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
rs137852769 0.827 0.280 2 26195184 missense variant C/G snv 1.2E-03 1.0E-03 7
rs1051861187 0.827 0.080 7 87409385 missense variant A/G snv 6