ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.2578+9C>T

dbSNP: rs2139736658
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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 RCV001492415 SCV001697026 likely benign Hereditary spastic paraplegia 49 2023-10-13 criteria provided, single submitter clinical testing

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