ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.5678+3G>A

gnomAD frequency: 0.00001  dbSNP: rs1060500826
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 RCV003766497 SCV000544042 likely benign not provided 2025-01-16 criteria provided, single submitter clinical testing
Mendelics RCV000476823 SCV001138863 likely benign Colorectal cancer, susceptibility to, 12 2019-05-28 criteria provided, single submitter clinical testing

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