ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.177G>C (p.Leu59=)

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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 RCV002711975 SCV003006074 likely benign Hereditary spastic paraplegia 49 2022-01-16 criteria provided, single submitter clinical testing

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