ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.1047C>T (p.His349=)

gnomAD frequency: 0.00036  dbSNP: rs148357976
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001518367 SCV001727044 benign Immunodeficiency 14 2025-01-19 criteria provided, single submitter clinical testing

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