ClinVar Miner

Submissions for variant NM_000038.6(APC):c.933+7G>C

gnomAD frequency: 0.00002  dbSNP: rs369087912
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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 RCV002544941 SCV001629667 likely benign Familial adenomatous polyposis 1 2024-10-15 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002544941 SCV004933494 likely benign Familial adenomatous polyposis 1 2024-02-29 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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