ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.*412G>A

gnomAD frequency: 0.00003  dbSNP: rs972128957
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Aziz Sancar Institute of Experimental Medicine, Istanbul University RCV000736007 SCV000611860 likely pathogenic Somatotroph adenoma 2017-12-05 criteria provided, single submitter research A novel variant associated with clinical findings.

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.