ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.21(chr22:18912403-21431174)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV000767629 SCV000898251 pathogenic DiGeorge Syndrome 2018-11-01 criteria provided, single submitter clinical testing
Department of Molecular and Human Genetics, Baylor College of Medicine RCV001195119 SCV001334076 pathogenic DiGeorge Syndrome 2020-04-16 no assertion criteria provided clinical testing

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