ClinVar Miner

Submissions for variant GRCh37/hg19 17q12(chr17:34807069-36284994)x1

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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 RCV001801177 SCV002047389 likely pathogenic Chromosome 17q12 deletion syndrome 2021-01-14 criteria provided, single submitter clinical testing

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