ClinVar Miner

Submissions for variant NM_001199753.2(CPT1C):c.438C>A (p.Pro146=)

dbSNP: rs372366841
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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 RCV000874538 SCV001016728 likely benign Hereditary spastic paraplegia 73 2023-05-04 criteria provided, single submitter clinical testing

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