Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1460548929
PRKCSH
0.925 0.040 19 11442432 missense variant A/G snv 4.0E-06 2
rs722782 1.000 0.040 8 566479 intergenic variant A/C;T snv 1
rs749856572
RAD51B
1.000 0.040 14 67835182 stop gained G/A;T snv 4.0E-06 1
rs1253615192
HTRA1 ; LOC105378525
0.925 0.040 10 122461959 missense variant C/G snv 7.0E-06 2
rs61755783
PRPH2
0.763 0.080 6 42721911 missense variant G/A snv 1.4E-05 11
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 6
rs151207349
PRKCSH
0.925 0.040 19 11441343 missense variant C/T snv 7.0E-04 5.7E-04 2
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 6
rs191281603
CFHR5
0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs35292876
CFH
0.851 0.040 1 196737512 synonymous variant C/T snv 1.0E-02 8.6E-03 4
rs140647181
LOC105374007
0.851 0.040 3 99461824 intergenic variant T/C snv 1.5E-02 4
rs187328863
KCNT2
0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs4151667
CFB ; CYP21A2
0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs9621532
SYN3
0.851 0.040 22 32688525 intron variant A/C snv 5.8E-02 4
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12 4
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs7803454
PILRA
0.851 0.040 7 100393925 intron variant C/T snv 0.14 4
rs3138141
RDH5 ; BLOC1S1-RDH5
0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4