Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs10399805 0.851 0.240 1 203186870 upstream gene variant G/A;T snv 7
rs2229542 0.925 0.160 7 134450869 missense variant T/C snv 1.3E-02 1.0E-02 3
rs946261 1.000 0.080 1 203188745 upstream gene variant C/T snv 0.47 2