ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.4150-12T>C

dbSNP: rs551697046
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698103 SCV000724569 likely benign not provided 2018-07-26 criteria provided, single submitter clinical testing
Counsyl RCV000662976 SCV000785956 likely benign Colorectal cancer, susceptibility to, 12 2018-01-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001698103 SCV002347109 benign not provided 2025-01-23 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257857 SCV002536835 benign Hereditary cancer-predisposing syndrome 2020-10-12 criteria provided, single submitter curation

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