Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4772
Gene Symbol: NFATC1
NFATC1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation 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
Entrez Id: 4772
Gene Symbol: NFATC1
NFATC1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation BEFREE We have previously shown that a tandem repeat in the intronic region of NFATC1 is associated with ventricular septal defects. 23226213

2012
Entrez Id: 4772
Gene Symbol: NFATC1
NFATC1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation 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
Entrez Id: 4772
Gene Symbol: NFATC1
NFATC1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.040 GeneticVariation 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