ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.3068-13C>T

gnomAD frequency: 0.00001  dbSNP: rs575387524
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001703694 SCV000522208 likely benign not provided 2021-03-09 criteria provided, single submitter clinical testing
Counsyl RCV000663268 SCV000786500 likely benign Colorectal cancer, susceptibility to, 10 2018-05-14 criteria provided, single submitter clinical testing
Invitae RCV000663268 SCV002438739 likely benign Colorectal cancer, susceptibility to, 10 2024-01-28 criteria provided, single submitter clinical testing

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