ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.2718-42A>C

dbSNP: rs759314322
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
GeneDx RCV001678067 SCV001895003 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003321865 SCV004027020 benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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