ClinVar Miner

Submissions for variant GRCh38/hg38 9p23-22.3(chr9:13974416-14286260)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Human Genetics, University Hospital Magdeburg RCV000681558 SCV000809032 pathogenic Dolichocephaly; Intellectual disability 2018-08-22 no assertion criteria provided clinical testing

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