ClinVar Miner

Submissions for variant NM_001199753.2(CPT1C):c.1758T>C (p.Tyr586=)

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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 RCV002786028 SCV003025003 likely benign Hereditary spastic paraplegia 73 2022-12-21 criteria provided, single submitter clinical testing

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