ClinVar Miner

Submissions for variant NM_006459.4(ERLIN1):c.564-20T>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 RCV003756412 SCV004534827 likely benign Hereditary spastic paraplegia 62 2023-04-30 criteria provided, single submitter clinical testing

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