ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.952-9_952-6del

dbSNP: rs565236204
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001848274 SCV002105980 uncertain significance Hereditary spastic paraplegia 2020-08-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693776 SCV005194329 uncertain significance not provided criteria provided, single submitter not provided

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