ClinVar Miner

Submissions for variant GRCh37/hg19 1q21.1(chr1:145382123-145792051)

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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 RCV003319572 SCV004023346 pathogenic Chromosome 1q21.1 deletion syndrome no assertion criteria provided clinical testing

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