ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1665-44C>A

gnomAD frequency: 0.00167  dbSNP: rs141589697
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001682919 SCV001898264 benign not provided 2020-04-01 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316158 SCV004016566 likely benign Cowden syndrome 5 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001682919 SCV005302479 benign not provided criteria provided, single submitter not provided
University of Washington Department of Laboratory Medicine, University of Washington RCV000209425 SCV000265356 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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