Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs4240624 0.882 0.040 8 9326721 intron variant G/A snv 0.87 5