ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.352+40A>G

gnomAD frequency: 0.26066  dbSNP: rs3729674
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001644914 SCV001859749 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001644914 SCV005302466 benign not provided criteria provided, single submitter not provided
Faculté Pluridciplinaire Nador, Université Mohamed Premier RCV001250964 SCV001250947 uncertain significance Squamous cell lung carcinoma 2020-05-05 no assertion criteria provided clinical testing

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