ClinVar Miner

Submissions for variant GRCh37/hg19 Xp21.1-11.4(chrX:37550041-37645092)

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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 RCV002280606 SCV002568873 pathogenic Granulomatous disease, chronic, X-linked no assertion criteria provided clinical testing

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