ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.3583-12dup

dbSNP: rs766426579
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 RCV001705270 SCV000289335 likely benign not provided 2024-01-12 criteria provided, single submitter clinical testing
GeneDx RCV001705270 SCV000570219 likely benign not provided 2023-11-06 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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