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: rs1064795747
rs1064795747
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.010 GeneticVariation BEFREE We conclude that the I157T variant of CHEK2 increases the risk of colorectal cancer among MMR-negative, HNPCC/HNPCC-related families in Poland. 19876921 2010