Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs961150162 7 55198779 missense variant G/A;C snv 3
rs869320694 0.742 0.520 8 38414790 missense variant T/C snv 16
rs3136797 0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs557263543 8 38412508 3 prime UTR variant C/T snv 3
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs200863613 0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs1057519771 1.000 0.080 9 130872201 missense variant G/C snv 2
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs367597251 0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs55958994 0.925 0.080 12 52907235 intron variant C/T snv 0.12 3
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
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs767808984 0.851 0.160 14 36520098 missense variant C/G;T snv 1.3E-05 9
rs2016347 0.790 0.160 15 98960571 3 prime UTR variant G/A;T snv 9