ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.1758G>A (p.Arg586=)

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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 RCV002942416 SCV003269322 likely benign Hereditary spastic paraplegia 49 2022-04-12 criteria provided, single submitter clinical testing

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