ClinVar Miner

Submissions for variant NM_013266.4(CTNNA3):c.843+12G>C

dbSNP: rs767324815
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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 RCV002179261 SCV002485049 likely benign Arrhythmogenic right ventricular dysplasia 13 2022-02-05 criteria provided, single submitter clinical testing

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