ClinVar Miner

Submissions for variant GRCh38/hg38 21q11.2-21.3(chr21:14000146-27785985)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Genetics, University of Pavia RCV000225561 SCV000239861 pathogenic Monosomy 21 2015-07-01 no assertion criteria provided clinical testing

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