ClinVar Miner

Submissions for variant NM_001382430.1(AKT1):c.1086C>T (p.Leu362=)

dbSNP: rs2140901197
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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 RCV002122460 SCV002394891 likely benign Cowden syndrome 6 2022-08-31 criteria provided, single submitter clinical testing

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