ClinVar Miner

Submissions for variant NM_001382430.1(AKT1):c.43C>A (p.Arg15=)

dbSNP: rs2141006801
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001494531 SCV001699189 likely benign Cowden syndrome 6 2023-05-15 criteria provided, single submitter clinical testing

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