ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.23(chr22:23720171-25065576)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Mendelian Genomics, University Medical Centre Ljubljana RCV000626496 SCV000747197 uncertain significance Cerebellar ataxia 2017-01-01 criteria provided, single submitter clinical testing

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