ClinVar Miner

Submissions for variant NM_013266.4(CTNNA3):c.1978-9_1978-8del

gnomAD frequency: 0.00009  dbSNP: rs750667259
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001499995 SCV001704771 likely benign Arrhythmogenic right ventricular dysplasia 13 2021-12-02 criteria provided, single submitter clinical testing
GeneDx RCV000228400 SCV002004445 likely benign not provided 2020-07-15 criteria provided, single submitter clinical testing

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