ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.369+17C>T

dbSNP: rs2143997153
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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 RCV002094064 SCV002426411 likely benign Familial meningioma 2023-01-05 criteria provided, single submitter clinical testing

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