ClinVar Miner

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

dbSNP: rs571894716
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003766984 SCV000637082 likely benign not provided 2024-11-24 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001841456 SCV001342542 likely benign Cardiac arrhythmia 2019-04-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001841456 SCV004827066 likely benign Cardiac arrhythmia 2023-12-13 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003766984 SCV005877091 likely benign not provided 2024-07-14 criteria provided, single submitter clinical testing

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