ClinVar Miner

Submissions for variant NM_001382430.1(AKT1):c.47-8G>A

dbSNP: rs770565457
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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 RCV002115407 SCV002393352 likely benign Cowden syndrome 6 2023-11-08 criteria provided, single submitter clinical testing

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