ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.2508G>A (p.Ala836=)

dbSNP: rs1889724315
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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 RCV001403427 SCV001605297 likely benign Hereditary spastic paraplegia 49 2022-10-27 criteria provided, single submitter clinical testing

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