ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.81A>G (p.Gly27=)

dbSNP: rs2144009232
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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 RCV001490754 SCV001695325 likely benign Familial meningioma 2019-10-09 criteria provided, single submitter clinical testing

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