ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.501A>G (p.Gly167=)

dbSNP: rs759123413
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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 RCV002182198 SCV002333688 likely benign Familial meningioma 2021-06-22 criteria provided, single submitter clinical testing

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