ClinVar Miner

Submissions for variant NM_014946.4(SPAST):c.1224T>G (p.Ala408=)

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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 RCV002770428 SCV003019702 likely benign Hereditary spastic paraplegia 4 2024-11-11 criteria provided, single submitter clinical testing

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