ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1959-14T>C

dbSNP: rs2149857355
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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. RCV004566030 SCV004933537 likely benign Familial adenomatous polyposis 1 2024-03-08 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 RCV004566030 SCV005846946 likely benign Familial adenomatous polyposis 1 2024-12-23 criteria provided, single submitter clinical testing

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