MSH2, mutS homolog 2, 4436

N. diseases: 490; N. variants: 777
Disease: Colorectal Carcinoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1114167806
rs1114167806
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.700 CausalMutation CLINVAR