ClinVar Miner

Submissions for variant GRCh37/hg19 10p13(chr10:16949550-16975190)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 Laboratory of Genetics and Genomics, Cincinnati Children's Hospital Medical Center RCV000749515 SCV000877851 benign not provided 2013-04-22 no assertion criteria provided clinical testing

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