ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.352+11A>G

gnomAD frequency: 0.00033  dbSNP: rs201605394
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001579637 SCV001872988 likely benign not provided 2021-02-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072288 SCV002487996 likely benign Cowden syndrome 2024-06-21 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579637 SCV001807968 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001579637 SCV001920746 likely benign not provided no assertion criteria provided clinical testing

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