rs575109631, CFH

N. diseases: 2
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 0.925 0.200 1 196745862 missense variant A/G snv 4.0E-06 0.700 1.000 8 1997 2006
Atypical Hemolytic Uremic Syndrome
CUI: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
42 0.925 0.200 1 196745862 missense variant A/G snv 4.0E-06 0.010 1.000 1 2019 2019