rs181317402, CERS1;GDF1

N. diseases: 3
Disease: Tetralogy of Fallot ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
0.010 GeneticVariation BEFREE Analysis of combined samples revealed a significant association in genotype and allele frequencies of rs181317402 T/G polymorphism between CHD cases in overall or ventricular septal defects or Tetralogy of Fallot and the control group. rs181317402 allele G polymorphism was significantly associated with a decreased risk of CHD. 31171573 2019