rs16939660, ALDH1A2

N. diseases: 2
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 We determined that the SNP rs16939660, previously associated with spina bifida and observed in patients with TOF, does not affect splicing. 19886994 2009