ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.952-8_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 RCV001848273 SCV002105979 uncertain significance Hereditary spastic paraplegia 2022-01-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693775 SCV005194307 uncertain significance not provided criteria provided, single submitter not provided

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