Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs2740488 0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs17231506 0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 7
rs2043085 0.827 0.080 15 58388755 intron variant T/C snv 0.54 6
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs1142 0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 5
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 5
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 5
rs73036519 0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs3138141 0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5
rs11080055 0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 4
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4