ClinVar Miner

Submissions for variant NM_000038.6(APC):c.646-7A>G

dbSNP: rs758518804
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003773884 SCV002448365 likely benign Familial adenomatous polyposis 1 2021-11-23 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004804387 SCV005423897 likely benign Classic or attenuated familial adenomatous polyposis 2024-03-24 criteria provided, single submitter clinical testing

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