ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.2016-29A>T

gnomAD frequency: 0.00242  dbSNP: rs374926790
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987363 SCV001136642 benign Cowden syndrome 1 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001655655 SCV001869359 benign not provided 2020-04-01 criteria provided, single submitter clinical testing

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