ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.897G>A (p.Arg299=)

dbSNP: rs754006294
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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 RCV002093664 SCV002387237 likely benign Familial meningioma 2021-11-02 criteria provided, single submitter clinical testing

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