Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7803454 0.851 0.040 7 100393925 intron variant C/T snv 0.14 4
rs67538026 0.851 0.040 19 1031439 intron variant C/T snv 0.37 4
rs2740488 0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs1142 0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs2285714 0.882 0.040 4 109717654 synonymous variant C/T snv 0.37 0.31 3
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 6
rs61941274 0.827 0.160 12 111694806 intron variant G/A;T snv 5
rs1999930
FRK
0.882 0.040 6 116065971 intergenic variant C/A;G;T snv 3
rs2736911 0.882 0.120 10 122454839 stop gained C/A;T snv 4.0E-06; 0.13 3
rs10490924 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs3750847 0.882 0.040 10 122455905 intron variant C/T snv 0.23 4
rs3750846 0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs3793917 0.882 0.040 10 122459759 non coding transcript exon variant C/G snv 0.23 3
rs11200638 0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs2284665 0.882 0.040 10 122467114 intron variant G/A;T snv 3
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1136287 0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs187328863 0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9