ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.4296+9C>A

dbSNP: rs572950088
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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 RCV005208936 SCV001708504 likely benign not provided 2024-09-18 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals RCV001503648 SCV004244262 likely benign Brugada syndrome 2023-12-20 no assertion criteria provided clinical testing

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