Gene: MSH6 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060502901
rs1060502901
MSH6 ; FBXO11
G 0.700 GeneticVariation CLINVAR Population-based molecular screening for Lynch syndrome: implications for personalized medicine. 23733757

2013
dbSNP: rs1064793489
rs1064793489
MSH6 ; FBXO11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1064794075
rs1064794075
MSH6
AG 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167695
rs1114167695
MSH6 ; FBXO11
GAT 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167697
rs1114167697
MSH6 ; FBXO11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167723
rs1114167723
MSH6 ; FBXO11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167725
rs1114167725
MSH6 ; FBXO11
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167729
rs1114167729
MSH6 ; FBXO11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167734
rs1114167734
MSH6
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1302369946
rs1302369946
MSH6 ; FBXO11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1316409501
rs1316409501
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. 18301448

2008
dbSNP: rs1316409501
rs1316409501
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants. 22102614

2012
dbSNP: rs1316409501
rs1316409501
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes. 16203774

2005
dbSNP: rs1316409501
rs1316409501
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR Functional analysis in mouse embryonic stem cells reveals wild-type activity for three MSH6 variants found in suspected Lynch syndrome patients. 24040339

2013
dbSNP: rs1316409501
rs1316409501
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity. 28531214

2017
dbSNP: rs1316409501
rs1316409501
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment. 22851212

2012
dbSNP: rs1553332776
rs1553332776
MSH6 ; FBXO11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553333168
rs1553333168
MSH6 ; FBXO11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553333644
rs1553333644
MSH6 ; FBXO11
GTTATTCAAAAGGGACATAGA 0.700 GeneticVariation CLINVAR

dbSNP: rs1553333753
rs1553333753
MSH6 ; FBXO11
ATTAT 0.700 GeneticVariation CLINVAR

dbSNP: rs1553408467
rs1553408467
MSH6
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553412912
rs1553412912
MSH6 ; FBXO11
GT 0.700 GeneticVariation CLINVAR

dbSNP: rs1558666177
rs1558666177
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR

dbSNP: rs182024561
rs182024561
MSH6 ; FBXO11
G 0.700 GeneticVariation CLINVAR

dbSNP: rs267608098
rs267608098
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR