ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.1028-10G>T

dbSNP: rs2037063345
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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 RCV002198640 SCV002485877 likely benign Familial meningioma 2021-10-18 criteria provided, single submitter clinical testing

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