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
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs4757268 0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs1801058 0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs5351 0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228611 0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs3748024 0.925 0.080 2 112588836 3 prime UTR variant C/G snv 0.41 0.35 3
rs225014 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs1799722 0.882 0.240 14 96204802 5 prime UTR variant C/T snv 0.41 0.39 4