ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.5415T>C (p.Phe1805=)

dbSNP: rs2125979289
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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 RCV001407840 SCV001609822 likely benign Brugada syndrome 2020-06-21 criteria provided, single submitter clinical testing

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