Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 16
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs6983561 0.925 0.080 8 127094635 intron variant A/C snv 0.17 3
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs1207692596
MPO
0.925 0.080 17 58280438 missense variant G/A;T snv 3
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 9
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs17632542 0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 4
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 66
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55