ClinVar Miner

Submissions for variant NM_203447.3(DOCK8):c.4886+3A>G (rs2360712)

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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 RCV000150515 SCV000197701 benign not specified 2013-02-21 criteria provided, single submitter clinical testing 4886+3A>G in intron 38 of DOCK8: This variant is not expected to have clinical s ignificance because it has been identified in 48.5% (2135/4406) of African Ameri can chromosomes from a broad population by the NHLBI Exome Sequencing Project (h ttp://evs.gs.washington.edu/EVS; dbSNP rs2360712).
PreventionGenetics,PreventionGenetics RCV000150515 SCV000317177 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000309557 SCV000480327 benign Hyper-IgE syndrome 2016-06-14 criteria provided, single submitter clinical testing

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