ClinVar Miner

Submissions for variant NM_013266.4(CTNNA3):c.2647T>C (p.Leu883=)

gnomAD frequency: 0.00002  dbSNP: rs751884087
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001410773 SCV001612824 likely benign Arrhythmogenic right ventricular dysplasia 13 2024-01-22 criteria provided, single submitter clinical testing

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