ClinVar Miner

Submissions for variant GRCh37/hg19 2q34(chr2:211708028-212975940)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003986298 SCV004802427 uncertain significance not specified criteria provided, single submitter clinical testing

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