ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.3474C>T (p.Ile1158=)

dbSNP: rs145568435
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002927368 SCV003260922 likely benign Brugada syndrome 2021-12-21 criteria provided, single submitter clinical testing

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