ClinVar Miner

Submissions for variant NM_014687.4(RUBCN):c.1262-1G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003234872 SCV003932845 uncertain significance Autosomal recessive spinocerebellar ataxia 15 criteria provided, single submitter clinical testing

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