ClinVar Miner

Submissions for variant GRCh37/hg19 17q12(chr17:34752221-36105007)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 RCV003329520 SCV004036105 pathogenic Chromosome 17q12 deletion syndrome 2022-10-05 criteria provided, single submitter clinical testing

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