ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.225G>A (p.Arg75=)

dbSNP: rs2143999523
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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 RCV002197343 SCV002356958 likely benign Familial meningioma 2021-11-19 criteria provided, single submitter clinical testing

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