ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2(chr15:22770421-23283811)x1

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003987080 SCV004802012 pathogenic not specified criteria provided, single submitter clinical testing
ISCA site 1 RCV000510306 SCV000585588 conflicting data from submitters See cases 2014-12-02 no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)
Cytogenetics, Genetics Associates, Inc. RCV002285078 SCV002569177 uncertain significance See cases no assertion criteria provided clinical testing

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