ClinVar Miner

Submissions for variant NM_000038.6(APC):c.7658_7661dup (p.His2554fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV003484510 SCV004229066 likely pathogenic Familial adenomatous polyposis 1 2023-11-16 criteria provided, single submitter clinical testing

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