ClinVar Miner

Submissions for variant GRCh37/hg19 4q35.2(chr4:188424331-189928653)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cytogenetics Laboratory, University of Washington RCV000203436 SCV000258568 likely benign See cases 2015-07-24 criteria provided, single submitter clinical testing

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