ClinVar Miner

Submissions for variant NM_152415.3(VPS37A):c.901-18T>C

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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 RCV002928555 SCV003269120 likely benign Hereditary spastic paraplegia 53 2025-01-20 criteria provided, single submitter clinical testing

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