ClinVar Miner

Submissions for variant NM_145064.3(STAC3):c.335-9T>C

gnomAD frequency: 0.00002  dbSNP: rs757163562
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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 RCV002080713 SCV002380676 likely benign Bailey-Bloch congenital myopathy 2023-12-19 criteria provided, single submitter clinical testing

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