ClinVar Miner

Submissions for variant NM_000052.7(ATP7A):c.2497A>G (p.Ser833Gly)

dbSNP: rs2149096859
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000012548 SCV000032782 pathogenic Cutis laxa, X-linked 1994-10-01 no assertion criteria provided literature only
Inherited Neuropathy Consortium Ii, University Of Miami RCV000012548 SCV004012053 uncertain significance Cutis laxa, X-linked 2016-01-06 no assertion criteria provided literature only

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.