ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.2235-17G>T

dbSNP: rs760680625
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002102536 SCV002387669 likely benign Immunodeficiency 14 2022-06-09 criteria provided, single submitter clinical testing

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