ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.2717+9C>T

dbSNP: rs760140187
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000231349 SCV000287590 likely benign Colorectal cancer, susceptibility to, 10 2023-12-14 criteria provided, single submitter clinical testing
Counsyl RCV000231349 SCV000488884 likely benign Colorectal cancer, susceptibility to, 10 2016-07-11 criteria provided, single submitter clinical testing

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