ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.21(chr22:18648866-21798907)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital RCV002280731 SCV002568996 pathogenic DiGeorge syndrome no assertion criteria provided clinical testing

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