Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs1864163 0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs6857 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs2269426 0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs17231506 0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 5
rs2043085 0.827 0.080 15 58388755 intron variant T/C snv 0.54 4
rs9391734 0.882 0.160 6 32130206 5 prime UTR variant G/A snv 0.11 4
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs6795735 0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs6680396
CFH
1.000 0.040 1 196663340 intron variant A/G snv 0.22 3
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 3
rs406936 0.882 0.240 6 31965384 intron variant G/A snv 0.19 3