ClinVar Miner

Submissions for variant GRCh37/hg19 11p15.5(chr11:1621232-2228572)

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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 RCV002280763 SCV002569030 pathogenic Beckwith-Wiedemann syndrome no assertion criteria provided clinical testing

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