ClinVar Miner

Submissions for variant GRCh37/hg19 1p36.33-36.22(chr1:849466-10258804)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital RCV002280717 SCV002568982 pathogenic Chromosome 1p36 deletion syndrome, proximal no assertion criteria provided clinical testing

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