MSH6, mutS homolog 6, 2956

N. diseases: 296; N. variants: 642
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042821
rs1042821
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
CUI: C0699790
Disease:
Colon Carcinoma
0.020 GeneticVariation BEFREE A study was conducted to examine whether MLH1 (-93G>A and Ile219Val) and MSH6 (Gly39Glu) polymorphisms were associated with risk of colon cancer in data from 1609 colon cancer cases and 1972 controls. 18523027 2009
dbSNP: rs1042821
rs1042821
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
CUI: C0699790
Disease:
Colon Carcinoma
0.020 GeneticVariation BEFREE In microsatellite stable tumors, homozygous carriers of the G39E polymorphism had an increased risk of CIMP+ colon cancer (odds ratio (OR) 2.2, 95% confidence interval (CI) 1.1, 4.2) and BRAF V600E mutation (OR 3.1, 95% CI 1.01, 9.7) in a case-control comparison. 19582761 2009
dbSNP: rs536562413
rs536562413
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0699790
Disease:
Colon Carcinoma
0.010 GeneticVariation BEFREE Statistically significant interactions were observed between: MLH1 -93G>A and smoking (MSI-negative colon cancer only, p value interaction: 0.005); and MLH1 Ile219Val and Western diet (p value interaction: 0.03). 18523027 2009
dbSNP: rs587780669
rs587780669
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0699790
Disease:
Colon Carcinoma
0.010 GeneticVariation BEFREE Statistically significant interactions were observed between: MLH1 -93G>A and smoking (MSI-negative colon cancer only, p value interaction: 0.005); and MLH1 Ile219Val and Western diet (p value interaction: 0.03). 18523027 2009