ClinVar Miner

Submissions for variant GRCh37/hg19 17q11.2-12(chr17:30572862-35843988)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Rehabilitation Medicine, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea RCV003319594 SCV004023330 pathogenic Chromosome 17q12 deletion syndrome no assertion criteria provided clinical testing

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