ClinVar Miner

Submissions for variant NM_018075.5(ANO10):c.1669-2A>T

dbSNP: rs797045240
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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 RCV000193009 SCV000246416 pathogenic Autosomal recessive spinocerebellar ataxia 10 2014-06-27 criteria provided, single submitter clinical testing

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