ClinVar Miner

Submissions for variant NM_000038.6(APC):c.423-5A>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004566285 SCV004931479 likely benign Familial adenomatous polyposis 1 2024-02-23 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.
Labcorp Genetics (formerly Invitae), Labcorp RCV004566285 SCV005757310 likely benign Familial adenomatous polyposis 1 2024-07-06 criteria provided, single submitter clinical testing

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