ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1313-19T>C

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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 RCV004374041 SCV004515009 likely benign Familial adenomatous polyposis 1 2023-01-16 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004374041 SCV004932948 likely benign Familial adenomatous polyposis 1 2024-03-01 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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