Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11112872 1.000 0.040 12 106111556 intron variant T/G snv 0.28 1
rs12449783 1.000 0.040 17 30200635 intron variant A/C;T snv 1
rs2297706 1.000 0.040 1 109914244 intron variant C/A;T snv 0.22 0.25 1
rs333967 1.000 0.040 1 109917151 intron variant C/T snv 0.28 1
rs5906435 1.000 0.040 X 47589011 intron variant C/G;T snv 1
rs73318382 1.000 0.040 5 160467536 intron variant A/C snv 5.4E-02 1
rs7762544 0.882 0.040 6 41411577 intergenic variant G/A snv 0.81 3
rs1595009 1.000 0.040 4 73968939 intergenic variant C/T snv 0.61 1
rs1027009063 0.925 0.040 2 8802974 stop gained G/A snv 2
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
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19