ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.931-9G>C (rs28730669)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000552428 SCV000604661 benign Immunodeficiency 14 2018-09-06 criteria provided, single submitter clinical testing
Invitae RCV000552428 SCV000653780 benign Immunodeficiency 14 2019-12-31 criteria provided, single submitter clinical testing

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