ClinVar Miner

Submissions for variant NM_018075.5(ANO10):c.306C>A (p.Tyr102Ter)

dbSNP: rs1210764379
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501690 SCV000593207 pathogenic Autosomal recessive spinocerebellar ataxia 10 2015-09-02 criteria provided, single submitter clinical testing

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