ClinVar Miner

Submissions for variant NM_001382430.1(AKT1):c.1172+10G>A

gnomAD frequency: 0.00001  dbSNP: rs200702576
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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 RCV001441652 SCV001644583 likely benign Cowden syndrome 6 2021-08-03 criteria provided, single submitter clinical testing

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