ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1627-19A>G

dbSNP: rs2149816691
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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 RCV004565210 SCV002376246 likely benign Familial adenomatous polyposis 1 2021-10-31 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004565210 SCV004933152 likely benign Familial adenomatous polyposis 1 2024-03-06 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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