ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1664+18G>A

dbSNP: rs104886001
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003753088 SCV004406521 likely benign Cowden syndrome 2023-08-28 criteria provided, single submitter clinical testing
Laboratory of Translational Genomics, National Cancer Institute RCV000119358 SCV000154255 not provided Familial cancer of breast no assertion provided not provided

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