Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1152888 1.000 0.080 12 66211448 missense variant A/C;G snv 4.0E-06; 0.87 1
rs3210908 1.000 0.080 11 406483 missense variant T/A;C snv 0.84 1
rs1061501 0.851 0.200 11 614864 synonymous variant C/T snv 0.83 0.85 4
rs887369 1.000 0.080 X 30559729 synonymous variant A/C;T snv 0.82; 3.3E-05 1
rs2255336 0.827 0.200 12 10379727 missense variant T/C snv 0.81 0.74 5
rs630379 0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs535586 0.882 0.160 6 31892560 splice region variant T/A;C snv 0.77 3
rs659445 0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs437179 0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs708035 0.925 0.120 3 10234479 missense variant T/A snv 0.73 0.70 2
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1059702 0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs428073 1.000 0.080 12 118244946 missense variant C/G;T snv 0.72 3
rs2480256 1.000 0.080 10 133539010 3 prime UTR variant A/G;T snv 0.71 1
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs3803800 0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 7
rs2243188 0.851 0.200 1 206841127 intron variant A/C;T snv 0.69 4
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
rs3747517 0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 13