ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2(chr15:22770421-23195725)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Rehabilitation Medicine, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea RCV003319588 SCV004023347 pathogenic Chromosome 15q11.2 deletion syndrome no assertion criteria provided clinical testing

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