ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.486T>G (p.Ser162=)

dbSNP: rs1597746062
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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 RCV000918868 SCV001064191 likely benign Familial meningioma 2021-05-20 criteria provided, single submitter clinical testing

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