DisGeNET - a database of gene-disease associations

MSH6, mutS homolog 6, 2956

N. diseases: 296; N. variants: 642

Disease: Colorectal Carcinoma ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs3211299

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs61753793

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63749889

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63750804

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63750836

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63750878

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63750882

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63750895

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63750949

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63750998

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63751009

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63751098

Entrez Id:	2956
Gene Symbol:	MSH6

MSH6

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63751113

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63751121

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63751258

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs63751450

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

rs2020912

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.710

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs267608140

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs34374438

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs63749973

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs63750157

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs63750253

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs63750287

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs63750304

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012

dbSNP:

rs63750358

Entrez Id:	2956;80204
Gene Symbol:	MSH6;FBXO11

MSH6;FBXO11

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

22102614

2012