Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1635498 0.807 0.160 1 241881973 missense variant C/A;G;T snv 0.96 9
rs2043449 0.882 0.080 2 203251967 missense variant C/T snv 0.94 0.89 3
rs9915936 0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs1046175 0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs2230229 0.807 0.120 8 23191779 missense variant C/T snv 0.88 0.86 8
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs1043994 0.827 0.120 19 15192033 synonymous variant T/A;C snv 4.0E-06; 0.85 7
rs2229959 0.882 0.080 20 63350202 synonymous variant C/A;T snv 0.84; 1.3E-05 3
rs738792 0.827 0.240 22 23779191 missense variant C/T snv 0.84 0.80 6
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs3206824 0.827 0.160 11 11964514 missense variant T/C snv 0.78 0.78 6
rs9912300 0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs7969931 0.851 0.080 12 25089661 missense variant C/A;G snv 1.6E-05; 0.75 5
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1948 0.827 0.160 15 78625057 synonymous variant A/G;T snv 0.69 5
rs228729 0.827 0.120 1 7785635 intron variant T/C snv 0.69 0.69 5
rs1042711 0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
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