ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.1020+13G>A

gnomAD frequency: 0.00008  dbSNP: rs377072140
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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 RCV002115650 SCV002393569 likely benign Immunodeficiency 14 2023-10-23 criteria provided, single submitter clinical testing

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