ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.2389-9C>G

gnomAD frequency: 0.00001  dbSNP: rs552399406
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001082375 SCV000646554 likely benign Colorectal cancer, susceptibility to, 10 2023-12-27 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759946 SCV000889664 likely benign not provided 2020-01-23 criteria provided, single submitter clinical testing
GeneDx RCV000759946 SCV001774006 likely benign not provided 2018-10-19 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258958 SCV002534632 likely benign Hereditary cancer-predisposing syndrome 2021-04-19 criteria provided, single submitter curation

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