ClinVar Miner

Submissions for variant NM_004946.3(DOCK2):c.1606A>G (p.Lys536Glu)

dbSNP: rs1581078478
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987630 SCV001137022 uncertain significance DOCK2 deficiency 2019-05-28 criteria provided, single submitter clinical testing

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