ClinVar Miner

Submissions for variant NM_001145661.2(GATA2):c.333C>T (p.His111=) (rs148554346)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000249258 SCV000306837 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000469997 SCV000554438 benign Lymphedema, primary, with myelodysplasia; Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency 2017-12-01 criteria provided, single submitter clinical testing

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