ClinVar Miner

Submissions for variant GRCh37/hg19 10p12.31(chr10:19417181-19834795)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 Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington RCV001194514 SCV001364145 uncertain significance See cases 2019-08-01 criteria provided, single submitter clinical testing

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