Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs10490924 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs2306283 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs11200638 0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 11
rs7830 0.763 0.320 7 151012483 3 prime UTR variant G/T snv 0.38 0.32 11