ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.250+220G>A

gnomAD frequency: 0.18637  dbSNP: rs356667
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001195041 SCV001899473 benign not provided 2019-08-19 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001195041 SCV001365312 uncertain significance not provided 2020-02-28 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Arleen D. Auerbach.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.