ClinVar Miner

Submissions for variant NC_000002.12:g.85889045G>T

gnomAD frequency: 0.33112  dbSNP: rs28364795
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
Breakthrough Genomics, Breakthrough Genomics RCV001637013 SCV005243758 benign not provided criteria provided, single submitter not provided
GeneDx RCV001637013 SCV001851667 benign not provided 2018-07-27 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.