ClinVar Miner

List of variants in gene RIMS1 reported as uncertain significance for Cone-Rod Dystrophy, Dominant

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_014989.5(RIMS1):c.*1457dup rs886061718
NM_014989.5(RIMS1):c.*1705C>T rs886061722
NM_014989.5(RIMS1):c.*517dup rs201958591
NM_014989.5(RIMS1):c.*538C>T rs886061713
NM_014989.5(RIMS1):c.1382C>T (p.Ala461Val) rs886061706
NM_014989.5(RIMS1):c.4057A>G (p.Thr1353Ala) rs886061709
NM_014989.5(RIMS1):c.4259T>C (p.Val1420Ala) rs373553229
NM_014989.5(RIMS1):c.4618+20dup rs113359739

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.