ClinVar Miner

Submissions for variant GRCh37/hg19 7p21.2(chr7:16163218-16173482)x0

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Genetics and Genomics,Cincinnati Children's Hospital Medical Center RCV000746523 SCV000874859 benign not provided 2012-04-21 no assertion criteria provided clinical testing

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