ClinVar Miner

Submissions for variant NM_006459.4(ERLIN1):c.196-4C>G

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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 RCV003075519 SCV003469702 likely benign Hereditary spastic paraplegia 62 2022-03-18 criteria provided, single submitter clinical testing

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