ClinVar Miner

Submissions for variant NM_024334.3(TMEM43):c.813G>A (p.Gln271=)

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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 RCV002632659 SCV003504524 likely benign Arrhythmogenic right ventricular dysplasia 5 2024-02-26 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002632659 SCV004832003 likely benign Arrhythmogenic right ventricular dysplasia 5 2023-07-10 criteria provided, single submitter clinical testing

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