ClinVar Miner

Submissions for variant GRCh37/hg19 12q12(chr12:42871679-42898233)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Cytogenomics Laboratory,Laboratory for Precision Diagnostics, University of Washington RCV001194588 SCV001364235 likely pathogenic See cases 2019-06-21 criteria provided, single submitter clinical testing

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