Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs34811474 1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs4252548 1.000 0.040 19 55368304 missense variant C/T snv 2.1E-02 1.8E-02 3
rs4337252 1.000 0.040 15 73934424 intron variant G/C snv 0.52 2