ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.3088-510A>G

gnomAD frequency: 0.66985  dbSNP: rs6801957
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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 RCV001513528 SCV001721159 benign Brugada syndrome 2025-01-20 criteria provided, single submitter clinical testing
GeneDx RCV001720290 SCV001949479 benign not provided 2020-01-27 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 24642470, 22706305, 21076409, 29448912)

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