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: rs1553335247
rs1553335247
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C4748135
Disease:
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
G 0.800 CausalMutation CLINVAR
dbSNP: rs61753793
rs61753793
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.710 GeneticVariation UNIPROT
dbSNP: rs1023534466
rs1023534466
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1054003194
rs1054003194
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
TG 0.700 CausalMutation CLINVAR
dbSNP: rs1054003194
rs1054003194
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
TG 0.700 CausalMutation CLINVAR
dbSNP: rs1054003194
rs1054003194
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057517551
rs1057517551
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C1833477
Disease:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
AT 0.700 GeneticVariation CLINVAR
dbSNP: rs1057517551
rs1057517551
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
AT 0.700 CausalMutation CLINVAR
dbSNP: rs1057517551
rs1057517551
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
AT 0.700 CausalMutation CLINVAR
dbSNP: rs1057517552
rs1057517552
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C1833477
Disease:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057517763
rs1057517763
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057517763
rs1057517763
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060502875
rs1060502875
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
C 0.700 CausalMutation CLINVAR
dbSNP: rs1060502876
rs1060502876
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060502881
rs1060502881
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
G 0.700 CausalMutation CLINVAR
dbSNP: rs1060502881
rs1060502881
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
G 0.700 CausalMutation CLINVAR
dbSNP: rs1060502882
rs1060502882
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
G 0.700 CausalMutation CLINVAR
dbSNP: rs1060502886
rs1060502886
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR
dbSNP: rs1060502890
rs1060502890
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
G 0.700 CausalMutation CLINVAR
dbSNP: rs1060502891
rs1060502891
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
T 0.700 CausalMutation CLINVAR
dbSNP: rs1060502901
rs1060502901
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C2936783
Disease:
Colorectal cancer, hereditary nonpolyposis, type 1
G 0.700 CausalMutation CLINVAR
dbSNP: rs1060502902
rs1060502902
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060502903
rs1060502903
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
GAAGA 0.700 CausalMutation CLINVAR
dbSNP: rs1060502918
rs1060502918
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1060502918
rs1060502918
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms
T 0.700 CausalMutation CLINVAR