ClinVar Miner

Submissions for variant NM_031448.6(C19orf12):c.177G>T (p.Gly59=)

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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 RCV005143953 SCV005766117 likely benign Hereditary spastic paraplegia 43 2024-11-19 criteria provided, single submitter clinical testing

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