Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs7830 0.763 0.320 7 151012483 3 prime UTR variant G/T snv 0.38 0.32 11
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1049255 0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9