ClinVar Miner

Submissions for variant NM_001042424.3(NSD2):c.-29-6901dup

dbSNP: rs886059308
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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 RCV000383472 SCV000449019 uncertain significance 4p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing

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