ClinVar Miner

Submissions for variant NM_001145661.2(GATA2):c.480C>T (p.Thr160=) (rs199640729)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000254047 SCV000306838 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV001080911 SCV000554446 benign Lymphedema, primary, with myelodysplasia; Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency 2019-12-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory,University of Chicago RCV000254047 SCV000594910 likely benign not specified 2017-04-12 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000466722 SCV001132725 likely benign not provided 2015-07-27 criteria provided, single submitter clinical testing

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