ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.1243-6C>T

gnomAD frequency: 0.00001  dbSNP: rs761914051
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001087734 SCV001010959 likely benign Colorectal cancer, susceptibility to, 10 2024-01-08 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000869525 SCV001134624 uncertain significance not provided 2018-12-03 criteria provided, single submitter clinical testing

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