Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs6795735 0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs2278426 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs9931989 16 28894763 intron variant G/C snv 0.68 3
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs1254319 1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs459193 0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs1128249 1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs9515201 0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs6861681 5 173935455 intron variant G/A snv 0.22 1
rs6942652 7 121249218 intron variant G/C;T snv 1
rs7647305 1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs11724804 0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs1011731 1 172377408 intron variant G/A snv 0.46 1