Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2266959 0.776 0.200 22 21568615 intron variant G/T snv 0.18 9
rs7137828 0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 7
rs2476491 0.776 0.240 10 6053447 intron variant A/T snv 0.25 8
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25