ClinVar Miner

Submissions for variant NM_018075.5(ANO10):c.1293+9A>G (rs7616708)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000601670 SCV000744189 benign Spinocerebellar ataxia, autosomal recessive 10 2015-09-21 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000601670 SCV000734279 benign Spinocerebellar ataxia, autosomal recessive 10 no assertion criteria provided clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000357200 SCV000444330 benign Autosomal recessive cerebellar ataxia 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000252832 SCV000313135 benign not specified criteria provided, single submitter clinical testing

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