Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs3785356 0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs9979383 0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs34173062 8 144103704 missense variant G/A;C snv 7.3E-02 3