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
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs4586 0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs379489
CFH
0.851 0.200 1 196724321 intron variant A/G snv 0.65 4