ClinVar Miner

Submissions for variant NM_005154.5(USP8):c.2896-8dup

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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 RCV005144297 SCV005767362 benign Hereditary spastic paraplegia 2024-02-14 criteria provided, single submitter clinical testing

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