CTNNA3, catenin alpha 3, 29119

N. diseases: 73; N. variants: 33
Disease: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777134
rs587777134
Entrez Id: 29119
Gene Symbol: CTNNA3
CTNNA3
CUI: C3810138
Disease:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13 		0.800 GeneticVariation UNIPROT Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy. 23136403 2013
dbSNP: rs587777134
rs587777134
Entrez Id: 29119
Gene Symbol: CTNNA3
CTNNA3
CUI: C3810138
Disease:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13 		T 0.800 CausalMutation CLINVAR