ClinVar Miner

Submissions for variant NM_001813.3(CENPE):c.2025G>A (p.Gln675=)

gnomAD frequency: 0.45048  dbSNP: rs2251634
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001579157 SCV001806581 benign Microcephaly 13, primary, autosomal recessive 2021-07-22 criteria provided, single submitter clinical testing
GeneDx RCV001713058 SCV001945926 benign not provided 2018-07-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001713058 SCV005302026 benign not provided criteria provided, single submitter not provided

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.