Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30