Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 7
rs7909519 0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 6
rs79893749 0.807 0.120 3 46212159 intron variant C/T snv 0.10 6
rs8129030 0.807 0.120 21 35340290 intron variant T/A;G snv 0.72 7
rs9532434 0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25