ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.369+10G>C

gnomAD frequency: 0.00012  dbSNP: rs199790447
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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 RCV000464965 SCV000557774 benign Familial meningioma 2024-01-22 criteria provided, single submitter clinical testing

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