ClinVar Miner

List of variants reported as benign for Lynch syndrome by University of Washington Department of Laboratory Medicine, University of Washington

Included ClinVar conditions (26):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000535.7(PMS2):c.993C>T (p.Cys331=) rs186577215 0.00009
NM_000179.3(MSH6):c.1809G>A (p.Lys603=) rs876660790 0.00001
NM_000535.7(PMS2):c.1398C>T (p.Gly466=) rs752666485 0.00001
NM_000251.3(MSH2):c.2355T>C (p.His785=) rs1114167840
NM_000535.7(PMS2):c.250+8G>A rs1057520511
NM_000535.7(PMS2):c.299A>G (p.Gln100Arg) rs747771951

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.