ClinVar Miner

Submissions for variant GRCh37/hg19 2q24.3-31.1(chr2:167996718-170671886)x1

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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 RCV000167568 SCV000218448 likely pathogenic See cases 2014-03-25 criteria provided, single submitter clinical testing patient also had deletion chr2:204032747-205890355 and deletion chr20:47682662-49884981

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