ClinVar Miner

Submissions for variant GRCh37/hg19 3q23-25.32(chr3:142729607-157921084)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001801182 SCV002047394 pathogenic Brachycephaly; Microcephaly; Attention deficit hyperactivity disorder 2021-06-30 criteria provided, single submitter clinical testing

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