ClinVar Miner

Submissions for variant NM_001042424.3(NSD2):c.*2012dup

dbSNP: rs766138833
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000401623 SCV000449105 uncertain significance 4p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing

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