Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2228467 1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs4761234 12 69338325 TF binding site variant T/C snv 0.36 5