ClinVar Miner

Submissions for variant NM_001160148.2(DDHD1):c.705C>T (p.Cys235=)

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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 RCV005202616 SCV005832828 likely benign Hereditary spastic paraplegia 28 2024-11-30 criteria provided, single submitter clinical testing

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