ClinVar Miner

Submissions for variant NM_013236.5(ATXN10):c.1173+54822_1173ATTCT[10_32]

dbSNP: rs60726084
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 RCV000001054 SCV000021204 benign Spinocerebellar ataxia type 10 2019-10-31 no assertion criteria provided literature only
GeneReviews RCV000001054 SCV000055894 non-pathogenic Spinocerebellar ataxia type 10 2012-09-20 no assertion criteria provided curation Converted during submission to Benign.

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.