ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.1686+11G>A

gnomAD frequency: 0.00001  dbSNP: rs534413213
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409342 SCV000489443 likely benign Colorectal cancer, susceptibility to, 10 2016-10-04 criteria provided, single submitter clinical testing
GeneDx RCV000417899 SCV000529742 likely benign not specified 2016-07-08 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.
Invitae RCV000409342 SCV002470442 likely benign Colorectal cancer, susceptibility to, 10 2024-01-26 criteria provided, single submitter clinical testing

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