ClinVar Miner

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

gnomAD frequency: 0.00033  dbSNP: rs201605394
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
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
Invitae RCV002072288 SCV002487996 likely benign Cowden syndrome 2023-11-24 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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.