ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by A.C.Camargo Cancer Center / LGBM, A.C.Camargo Cancer Center

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_000179.2(MSH6):c.1338A>T (p.Glu446Asp) rs587779211
NM_000179.2(MSH6):c.1932G>C (p.Arg644Ser) rs34938432
NM_000179.2(MSH6):c.3971_3973AGA[1] (p.Lys1325del) rs587779300

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.