ClinVar Miner

Submissions for variant GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)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 Medical Genetics and Applied Genomics, University Hospital Tübingen RCV003447845 SCV004175733 pathogenic Trisomy 12p 2023-12-12 criteria provided, single submitter clinical testing

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