ClinVar Miner

Submissions for variant NM_203447.3(DOCK8):c.1238A>G (p.Asn413Ser) (rs10970979)

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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 RCV000150508 SCV000197694 benign not specified 2013-02-21 criteria provided, single submitter clinical testing Asn413Ser in exon 11 of DOCK8: This variant is not expected to have clinical sig nificance because it has been identified in 30.9% (2659/8600) of European Americ an chromosomes from a broad population by the NHLBI Exome Sequencing Project (ht tp://evs.gs.washington.edu/EVS; dbSNP rs10970979).
PreventionGenetics,PreventionGenetics RCV000150508 SCV000317167 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000364547 SCV000479724 benign Hyper-IgE syndrome 2016-06-14 criteria provided, single submitter clinical testing

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