ClinVar Miner

Submissions for variant NM_001372.4(DNAH9):c.282C>T (p.Gly94=)

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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 RCV005207109 SCV005844320 likely benign not provided 2025-01-28 criteria provided, single submitter clinical testing

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