ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.1809G>C (p.Leu603=) (rs151278626)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000542806 SCV000653765 benign Immunodeficiency 14 2018-01-02 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000757615 SCV000885909 benign not provided 2017-08-17 criteria provided, single submitter clinical testing

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