ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.2295-57C>G

gnomAD frequency: 0.67874  dbSNP: rs2699889
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 RCV001693905 SCV001914797 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001693905 SCV005302489 benign not provided criteria provided, single submitter not provided

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