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: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2013 2013
dbSNP: rs1136287
rs1136287
8 0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 0.010 1.000 1 2008 2008