ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.715-12C>G

dbSNP: rs769970957
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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 RCV002137442 SCV002420126 likely benign Familial meningioma 2024-06-25 criteria provided, single submitter clinical testing

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