ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.1473+19G>A

dbSNP: rs1057517628
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411584 SCV000489648 likely benign Colorectal cancer, susceptibility to, 12 2016-10-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003766141 SCV002989530 likely benign not provided 2024-04-08 criteria provided, single submitter clinical testing

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