ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1743+18_1743+106del

dbSNP: rs1554082152
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000481935 SCV000571642 likely benign not specified 2017-04-10 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Color Diagnostics, LLC DBA Color Health RCV000584239 SCV000686851 likely benign Hereditary cancer-predisposing syndrome 2016-08-08 criteria provided, single submitter clinical testing
Invitae RCV003535761 SCV002331718 likely benign Familial adenomatous polyposis 1 2024-01-24 criteria provided, single submitter clinical testing

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