ClinVar Miner

Submissions for variant GRCh37/hg19 17q21.31(chr17:44160674-44293981)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center RCV000752064 SCV000880400 benign not provided 2014-05-23 no assertion criteria provided clinical testing

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