Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913059
rs121913059
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0398777
Disease:
Complement Factor H Deficiency
T 0.800 CausalMutation CLINVAR
dbSNP: rs121913059
rs121913059
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0398777
Disease:
Complement Factor H Deficiency
0.800 GeneticVariation UNIPROT