ClinVar Miner

Submissions for variant NM_001367805.3(KIF23):c.690A>G (p.Ile230Met)

gnomAD frequency: 0.00021  dbSNP: rs199679829
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000900896 SCV001045239 benign not provided 2024-11-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000900896 SCV004132752 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing KIF23: BS2
Mayo Clinic Laboratories, Mayo Clinic RCV000900896 SCV004227438 uncertain significance not provided 2022-05-10 criteria provided, single submitter clinical testing BS2
Breakthrough Genomics, Breakthrough Genomics RCV000900896 SCV005295284 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.