RAD51C, RAD51 paralog C, 5889

N. diseases: 162; N. variants: 96
Disease: Fanconi Anemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606997
rs267606997
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
CUI: C0015625
Disease:
Fanconi Anemia 		0.010 GeneticVariation BEFREE The RAD51C missense mutation p.Arg258His has previously been identified in a homozygous state in a patient with Fanconi anemia. 25154786 2015