ClinVar Miner

Submissions for variant NM_000533.5(PLP1):c.336C>T (p.Gly112=)

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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 RCV005120003 SCV005737249 likely benign Hereditary spastic paraplegia 2 2024-02-03 criteria provided, single submitter clinical testing

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