ClinVar Miner

Submissions for variant NC_012920.1:m.14771C>A

dbSNP: rs1556424489
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Neuroscience and Cell Biology, University of Coimbra, Portugal RCV000509010 SCV000492501 uncertain significance Autosomal recessive spinocerebellar ataxia 20 2016-12-22 no assertion criteria provided research

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