ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.1086C>A (p.Pro362=)

dbSNP: rs1379420694
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001506272 SCV001711191 likely benign Colorectal cancer, susceptibility to, 10 2024-04-23 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002255677 SCV002529044 likely benign Hereditary cancer-predisposing syndrome 2021-04-19 criteria provided, single submitter curation

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