ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.4659T>G (p.Pro1553=)

dbSNP: rs777765659
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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 RCV003539916 SCV000637159 likely benign not provided 2017-06-30 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV003999082 SCV004826213 likely benign Cardiac arrhythmia 2023-11-30 criteria provided, single submitter clinical testing

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