ClinVar Miner

Submissions for variant NM_001351169.2(NT5C2):c.772-5del

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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 RCV003583840 SCV004315631 benign Hereditary spastic paraplegia 45 2023-07-04 criteria provided, single submitter clinical testing

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