FANCC, FA complementation group C, 2176

N. diseases: 218; N. variants: 90
Disease: Fanconi Anemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs765551897
rs765551897
Entrez Id: 2176;84909
Gene Symbol: FANCC;AOPEP
FANCC;AOPEP
CUI: C0015625
Disease:
Fanconi Anemia 		TG 0.700 CausalMutation CLINVAR