ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2(chr15:22770421-23282799)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital RCV002280614 SCV002568881 uncertain significance Hypoplastic left heart syndrome 1 no assertion criteria provided clinical testing
Department of Rehabilitation Medicine, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea RCV003319573 SCV004023337 pathogenic Chromosome 15q11.2 deletion syndrome no assertion criteria provided clinical testing

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