ClinVar Miner

Submissions for variant NM_001322934.2(NFKB2):c.2146G>T (p.Asp716Tyr)

dbSNP: rs1589870841
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000988444 SCV001138162 uncertain significance Immunodeficiency, common variable, 10 2019-05-28 criteria provided, single submitter clinical testing

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