ClinVar Miner

Submissions for variant GRCh37/hg19 9p23-22.3(chr9:13106806-14639971)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 RCV000681559 SCV000809033 pathogenic Intellectual disability; Secondary microcephaly 2018-08-22 no assertion criteria provided clinical testing

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