Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121917887 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1458974438 0.807 0.080 19 1206957 missense variant G/A snv 9
rs1487151044 0.851 0.080 10 31510817 missense variant T/C snv 5
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs4647958 0.851 0.080 20 49984094 missense variant T/C snv 0.18 0.29 5
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104