ClinVar Miner

Submissions for variant NM_182758.4(WDR72):c.3149-30CT[13]

dbSNP: rs57737580
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV006441775 SCV007314244 benign not specified 2022-03-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494992 SCV002799894 likely benign Amelogenesis imperfecta hypomaturation type 2A3 2021-09-12 criteria provided, single submitter clinical testing

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. The submitted information has not been verified. If you have questions about the information contained on this website, please see a health care professional.