ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1095C>A (p.Leu365=)

dbSNP: rs370377886
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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 RCV003657207 SCV001668331 likely benign not provided 2024-07-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004804184 SCV005423973 likely benign Cardiac arrhythmia 2024-05-14 criteria provided, single submitter clinical testing

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