ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.423T>C (p.Ala141=)

dbSNP: rs2143996401
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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 RCV001484924 SCV001689348 likely benign Familial meningioma 2019-08-13 criteria provided, single submitter clinical testing

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