ClinVar Miner

Submissions for variant NM_016614.3(TDP2):c.635_636+2del

dbSNP: rs2127617300
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001783860 SCV002016868 likely pathogenic Spinocerebellar ataxia, autosomal recessive 23 2021-08-11 criteria provided, single submitter clinical testing

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