rs7650466, EPHA3

N. diseases: 7
Disease: Congenital Abnormality ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
0.010 GeneticVariation BEFREE The rs7650466 T allele could be associated with reduced risk of the malformation. 29932736 2018