ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2(chr15:22743127-23246000)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001801215 SCV002047427 pathogenic Chromosome 15q11.2 deletion syndrome 2021-11-10 criteria provided, single submitter clinical testing

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