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
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs1042031 0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs2278426 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs769455 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs2072183 0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 6