ClinVar Miner

Submissions for variant NR_039729.1(MIR2392):n.-10132_-1575del

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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 RCV000149430 SCV000190041 pathogenic Paternal uniparental disomy of chromosome 14 2010-06-01 no assertion criteria provided clinical testing

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