Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs2576178 0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9