ClinVar Miner

Submissions for variant NM_001371279.1(REEP1):c.411T>G (p.Ala137=)

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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 RCV005203214 SCV005836313 likely benign Hereditary spastic paraplegia 31 2024-09-23 criteria provided, single submitter clinical testing

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