rs3832879, FGF23

N. diseases: 2
Disease: Congenital Heart Defects ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
0.010 GeneticVariation BEFREE Each patient underwent evaluation of serum FGF23 levels and FGF23 genotype: the frequency of the c.212-37insC (rs3832879) polymorphism in intron 1 was examined and compared with sex, age at disease onset, fever duration, laboratory data, and occurrence of CaA. 24168888 2013