Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2292596 0.827 0.240 5 422840 missense variant C/G;T snv 0.38; 4.0E-06 7
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs2073618 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs3134069 0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs497309 0.882 0.240 6 31924707 intron variant A/C;G snv 5
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs8193037 0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19