ClinVar Miner

Submissions for variant GRCh37/hg19 2q23.1(chr2:149248413-149250399)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 Laboratory of Genetics and Genomics,Cincinnati Children's Hospital Medical Center RCV000740644 SCV000868980 benign not provided 2011-05-31 no assertion criteria provided clinical testing

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