ClinVar Miner

Submissions for variant GRCh37/hg19 12q24.21(chr12:116526663-116528428)x1

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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 RCV000750594 SCV000878930 benign not provided 2010-12-23 no assertion criteria provided clinical testing

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