ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.141C>G (p.Pro47=)

dbSNP: rs571894716
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000883259 SCV001702266 likely benign not provided 2020-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000883259 SCV001913977 benign not provided 2015-04-28 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003138 SCV004817154 likely benign Cardiac arrhythmia 2023-06-26 criteria provided, single submitter clinical testing

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