ClinVar Miner

Submissions for variant NM_000038.6(APC):c.*2AG[1]

dbSNP: rs758692443
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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 RCV001190311 SCV001357769 uncertain significance Hereditary cancer-predisposing syndrome 2019-02-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004789455 SCV005407378 benign Familial adenomatous polyposis 1 2024-09-30 criteria provided, single submitter clinical testing This variant is considered benign. This variant occurs in the non-coding 3' untranslated region of the gene, and is not expected to impact protein function.

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