ClinVar Miner

List of variants reported for not specified by Genetic Laboratory, Instituto Nacional de Cancer

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000179.3(MSH6):c.181G>A (p.Ala61Thr) rs1057524911
NM_000251.3(MSH2):c.2078G>A (p.Cys693Tyr) rs1057524909
NM_000535.6(PMS2):c.-77delA rs1057524913

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.