ClinVar Miner

Submissions for variant NM_203447.3(DOCK8):c.4785+6C>G (rs7036567)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000150514 SCV000197700 benign not specified 2013-02-21 criteria provided, single submitter clinical testing 4785+6C>G in intron 37 of DOCK8: This variant is not expected to have clinical s ignificance because it has been identified in 49.3% (2171/4406) of African Ameri can chromosomes from a broad population by the NHLBI Exome Sequencing Project (h ttp://; dbSNP rs7036567).
PreventionGenetics,PreventionGenetics RCV000150514 SCV000317176 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000403442 SCV000480326 benign Hyper-IgE syndrome 2016-06-14 criteria provided, single submitter clinical testing

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