Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
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
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs4240624 0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs4808199 1.000 0.040 19 19434290 intron variant G/A;T snv 0.19 5