ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.2155-6C>T

gnomAD frequency: 0.00002  dbSNP: rs112481714
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000229474 SCV000287555 likely benign Colorectal cancer, susceptibility to, 10 2024-01-27 criteria provided, single submitter clinical testing
GeneDx RCV000759943 SCV000720908 likely benign not provided 2021-05-10 criteria provided, single submitter clinical testing
Counsyl RCV000229474 SCV000785561 likely benign Colorectal cancer, susceptibility to, 10 2017-09-19 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759943 SCV000889659 benign not provided 2018-02-27 criteria provided, single submitter clinical testing
Mendelics RCV000229474 SCV001141151 likely benign Colorectal cancer, susceptibility to, 10 2019-05-28 criteria provided, single submitter clinical testing

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