ClinVar Miner

Submissions for variant GRCh37/hg19 Xq28(chrX:153247464-153522710)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 RCV003329535 SCV004036121 pathogenic Chromosome Xq28 duplication syndrome 2022-12-16 criteria provided, single submitter clinical testing

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