ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.708G>A (p.Pro236=)

gnomAD frequency: 0.00469  dbSNP: rs145697393
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000555455 SCV000653777 benign Immunodeficiency 14 2024-01-29 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001821613 SCV002069349 likely benign not specified 2021-11-09 criteria provided, single submitter clinical testing

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