ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.4620T>C (p.Asn1540=)

dbSNP: rs2125982760
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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 RCV001414261 SCV001616391 likely benign Brugada syndrome 2020-03-25 criteria provided, single submitter clinical testing

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