ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1146-38T>C

gnomAD frequency: 0.07929  dbSNP: rs3729682
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001643871 SCV001856061 benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001643871 SCV005302475 benign not provided criteria provided, single submitter not provided

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