ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.2787A>T (p.Val929=)

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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 RCV003651266 SCV004435847 likely benign Hereditary spastic paraplegia 49 2023-03-21 criteria provided, single submitter clinical testing

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