ClinVar Miner

Submissions for variant NM_001382430.1(AKT1):c.567+19G>T

dbSNP: rs2140916086
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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 RCV002180413 SCV002348938 likely benign Cowden syndrome 6 2021-10-26 criteria provided, single submitter clinical testing

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