Gene: MSH6 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2020912
rs2020912
MSH6 ; FBXO11
0.700 GeneticVariation UNIPROT Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. 14961575

2004
dbSNP: rs63750664
rs63750664
MSH6
0.700 GeneticVariation UNIPROT Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. 14961575

2004
dbSNP: rs63750741
rs63750741
MSH6 ; FBXO11
0.700 GeneticVariation UNIPROT Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. 14961575

2004
dbSNP: rs2020912
rs2020912
MSH6 ; FBXO11
0.700 GeneticVariation UNIPROT Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium? 11153917

2000
dbSNP: rs63750664
rs63750664
MSH6
0.700 GeneticVariation UNIPROT Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium? 11153917

2000
dbSNP: rs63750741
rs63750741
MSH6 ; FBXO11
0.700 GeneticVariation UNIPROT Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium? 11153917

2000
dbSNP: rs267608059
rs267608059
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR

dbSNP: rs63749843
rs63749843
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR

dbSNP: rs63749889
rs63749889
MSH6 ; FBXO11
0.700 GeneticVariation UNIPROT

dbSNP: rs63749999
rs63749999
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR

dbSNP: rs63751017
rs63751017
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR

dbSNP: rs786201042
rs786201042
MSH6
T 0.700 CausalMutation CLINVAR

dbSNP: rs876660943
rs876660943
MSH6 ; FBXO11
T 0.700 GeneticVariation CLINVAR

dbSNP: rs587781462
rs587781462
MSH6 ; FBXO11
0.010 GeneticVariation BEFREE To the best of our knowledge, this is the first description of MSH6 T767I pathogenic variant that could be associated with a hereditary endometrial cancer. 31100584

2019
dbSNP: rs63750111
rs63750111
MSH6 ; FBXO11
0.010 GeneticVariation BEFREE Unselected Jewish women with EC who were diagnosed from January 1982 to January 2008 were genotyped for the predominant mutations in Jewish individuals in BRCA1 (185delAG, 5382InsC, Tyr978X) BRCA2 (6174delT), MSH2 (A636P, 324delCA) and MSH6 (c.3984_3987dup). 20850175

2010