ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.2578+30_2578+42del

dbSNP: rs3831019
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704798 SCV000730006 benign not provided 2018-05-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001521435 SCV001730780 benign Hereditary spastic paraplegia 49 2025-02-03 criteria provided, single submitter clinical testing

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