ClinVar Miner

Submissions for variant NM_006459.4(ERLIN1):c.72C>T (p.Ser24=)

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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 RCV005123256 SCV005739816 likely benign Hereditary spastic paraplegia 62 2024-11-23 criteria provided, single submitter clinical testing

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