ClinVar Miner

Submissions for variant NM_024334.3(TMEM43):c.1075C>T (p.Leu359=)

dbSNP: rs767824014
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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 RCV001884858 SCV002158494 likely benign Arrhythmogenic right ventricular dysplasia 5 2023-10-03 criteria provided, single submitter clinical testing

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