ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.3641-8A>C

dbSNP: rs775147521
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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 RCV001423705 SCV001626286 likely benign Hereditary spastic paraplegia 49 2024-01-24 criteria provided, single submitter clinical testing

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