ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2(chr15:22770421-23277435)x1

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003987083 SCV004802015 pathogenic not specified criteria provided, single submitter clinical testing
Cytogenetics, Genetics Associates, Inc. RCV002285077 SCV002569167 uncertain significance See cases no assertion criteria provided clinical testing

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