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: rs62625015
rs62625015
CFH
1 1.000 0.160 1 196743544 missense variant C/G snv 3.9E-04 2.4E-04 0.700 1.000 8 1997 2006