NFATC1, nuclear factor of activated T cells 1, 4772

N. diseases: 161; N. variants: 23
Disease: Ventricular Septal Defects ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation group BEFREE As part of a larger study, high density single nucleotide polymorphism (SNP) scanning was used to explore the relationship between NFATc1 gene polymorphism and susceptibility to ventricular septal defect (VSD) in the Chinese Han population. 23286482 2013
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation group BEFREE We have previously shown that a tandem repeat in the intronic region of NFATC1 is associated with ventricular septal defects. 23226213 2012
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation group BEFREE The results suggested no association of the length variation of the intronic region in NFATC1 gene with VSD, atrial septal defect, and patent ductus arteriosus. 22032245 2012
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation group BEFREE A screen of a pool of 81 healthy, unrelated individuals showed no presence for the homozygous form of this allele, suggesting that NFATC1 is a potential VSD-susceptibility gene. 17110989 2006