ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.4291-11G>A

gnomAD frequency: 0.00011  dbSNP: rs369564167
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000412163 SCV000489042 likely benign Colorectal cancer, susceptibility to, 12 2016-08-05 criteria provided, single submitter clinical testing
GeneDx RCV001705538 SCV000715567 likely benign not provided 2019-12-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001705538 SCV002392456 likely benign not provided 2025-01-29 criteria provided, single submitter clinical testing

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