MSH2, mutS homolog 2, 4436

N. diseases: 490; N. variants: 777
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1114167882
rs1114167882
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TTTC 0.700 CausalMutation CLINVAR
dbSNP: rs587779146
rs587779146
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TTCATGTTGCAGAGC 0.700 CausalMutation CLINVAR
dbSNP: rs63750690
rs63750690
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TTA 0.700 CausalMutation CLINVAR
dbSNP: rs63751219
rs63751219
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TTA 0.700 CausalMutation CLINVAR
dbSNP: rs863225393
rs863225393
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TTA 0.700 CausalMutation CLINVAR
dbSNP: rs63750329
rs63750329
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TT 0.700 CausalMutation CLINVAR
dbSNP: rs267607696
rs267607696
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TGG 0.700 CausalMutation CLINVAR
dbSNP: rs1553367608
rs1553367608
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TGA 0.700 CausalMutation CLINVAR
dbSNP: rs1553348842
rs1553348842
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs1553369100
rs1553369100
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs193922375
rs193922375
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TG 0.700 CausalMutation CLINVAR Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome. 26248088 2015
dbSNP: rs193922375
rs193922375
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TG 0.700 CausalMutation CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183 2017
dbSNP: rs193922375
rs193922375
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs193922375
rs193922375
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TG 0.700 GeneticVariation CLINVAR
dbSNP: rs63750107
rs63750107
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs63750614
rs63750614
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TG 0.700 CausalMutation CLINVAR Immunosuppression and sebaceous tumors: a confirmed diagnosis of Muir-Torre syndrome unmasked by immunosuppressive therapy. 21550136 2011
dbSNP: rs63750614
rs63750614
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TG 0.700 CausalMutation CLINVAR Microsatellite instability and mutation analysis among southern Italian patients with colorectal carcinoma: detection of different alterations accounting for MLH1 and MSH2 inactivation in familial cases. 14504054 2003
dbSNP: rs63750614
rs63750614
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs63750614
rs63750614
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs786203604
rs786203604
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs864622261
rs864622261
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs1114167814
rs1114167814
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TC 0.700 CausalMutation CLINVAR
dbSNP: rs1553348896
rs1553348896
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TC 0.700 CausalMutation CLINVAR
dbSNP: rs1553348896
rs1553348896
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease:
Hereditary Nonpolyposis Colorectal Neoplasms 		TC 0.700 CausalMutation CLINVAR
dbSNP: rs63750496
rs63750496
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		TC 0.700 CausalMutation CLINVAR