ClinVar Miner

Submissions for variant GRCh37/hg19 Xp22.33-11.22(chrX:168546-52573789)

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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 RCV002280669 SCV002568932 pathogenic Turner syndrome no assertion criteria provided clinical testing

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