CFC1B, cripto, FRL-1, cryptic family 1B, 653275

N. diseases: 20; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2579433
rs2579433
Entrez Id: 653275
Gene Symbol: CFC1B
CFC1B
CUI: C0018817
Disease:
Atrial Septal Defects 		0.010 GeneticVariation BEFREE Furthermore, we found the previously characterized R78W polymorphism in another patient with type II atrial septal defect. 17072672 2007