rs121913056, CFH

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Complement Factor H Deficiency
CUI: C0398777
Disease: Complement Factor H Deficiency
9 1.000 0.160 1 196690194 missense variant T/A;G snv 4.0E-06; 4.0E-06 0.700 0