ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1408+17T>C

gnomAD frequency: 0.00001  dbSNP: rs748793009
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001184710 SCV001350749 likely benign Hereditary cancer-predisposing syndrome 2019-03-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067949 SCV002417979 likely benign Familial adenomatous polyposis 1 2024-05-26 criteria provided, single submitter clinical testing

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