ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.4935G>A (p.Leu1645=)

dbSNP: rs770115314
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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 RCV003773878 SCV002443469 likely benign not provided 2024-08-08 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004005451 SCV004827269 likely benign Cardiac arrhythmia 2023-08-15 criteria provided, single submitter clinical testing

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