ClinVar Miner

Submissions for variant NM_001382430.1(AKT1):c.828+10C>T

gnomAD frequency: 0.00006  dbSNP: rs370490407
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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 RCV000228128 SCV000288823 likely benign Cowden syndrome 6 2023-10-22 criteria provided, single submitter clinical testing

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