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-06 484
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 15
rs1494555 0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs539846
BMF
1.000 0.120 15 40105735 intron variant G/C;T snv 2