ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.4140G>A (p.Lys1380=)

dbSNP: rs1553695286
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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 RCV003654433 SCV000637148 likely benign not provided 2024-04-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV003999080 SCV004843842 likely benign Cardiac arrhythmia 2023-11-20 criteria provided, single submitter clinical testing

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