Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10494745
rs10494745
CFHR4 ; LOC105371675
2 1.000 0.040 1 196918327 missense variant G/A snv 8.0E-02 7.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs10754218
rs10754218
ZBTB41
2 1 197195884 intron variant G/A snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs10801582
rs10801582
CFHR5
2 1 196975227 upstream gene variant G/A snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs2786107
rs2786107
CRB1
1 1 197341647 intron variant G/T snv 0.80 0.700 1.000 1 2017 2017
dbSNP: rs419137
rs419137
CFH
1 1 196727745 intron variant G/T snv 0.92 0.700 1.000 1 2017 2017