Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
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
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs10490924 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs11200638 0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 10
rs9332739 0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 10
rs1136287 0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs641153 0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 7
rs61941274 0.827 0.160 12 111694806 intron variant G/A;T snv 5