ClinVar Miner

Submissions for variant GRCh37/hg19 1q21.1-21.2(chr1:145792051-148001265)

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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 RCV002280613 SCV002568880 pathogenic Hypoplastic left heart syndrome 1 no assertion criteria provided clinical testing

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