ClinVar Miner

Submissions for variant NM_003002.4(SDHD):c.*613T>C

gnomAD frequency: 0.93280  dbSNP: rs693441
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
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000037725 SCV000061387 benign not specified 2011-10-10 criteria provided, single submitter clinical testing This variant is classified as benign based on its high frequency in the general population (rs693441, MAF >3%).
Illumina Laboratory Services, Illumina RCV000287625 SCV000367359 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706465 SCV005231601 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.