ClinVar Miner

Submissions for variant NM_012073.5(CCT5):c.963G>A (p.Ala321=)

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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 RCV005193711 SCV005825079 likely benign Hereditary sensory and autonomic neuropathy with spastic paraplegia 2024-10-24 criteria provided, single submitter clinical testing

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