ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.234A>G (p.Arg78=)

dbSNP: rs2143999505
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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 RCV001486015 SCV001690464 likely benign Familial meningioma 2023-05-02 criteria provided, single submitter clinical testing

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