ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.2094C>T (p.Phe698=) (rs370548772)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000899481 SCV001043752 benign Immunodeficiency 14 2020-11-04 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000899481 SCV001470927 likely benign Immunodeficiency 14 2020-02-25 criteria provided, single submitter clinical testing

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