ClinVar Miner

Submissions for variant NC_000014.9:g.100824888_100829190delins100833642_100833702

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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 Molecular Endocrinology, National Research Institute for Child Health and Development RCV000149431 SCV000190042 pathogenic Paternal uniparental disomy of chromosome 14 2010-06-01 no assertion criteria provided clinical testing

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