MSH2, mutS homolog 2, 4436

N. diseases: 490; N. variants: 777
Disease: Breast Cancer, Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.310 Biomarker disease CLINGEN MSH2 rs2303425 Polymorphism is Associated with Early-Onset Breast Cancer in Taiwan. 26975740 2017
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.310 Biomarker disease CLINGEN The DNA mismatch repair gene hMSH2 is a potent coactivator of oestrogen receptor alpha. 15886699 2005
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.310 GeneticVariation disease BEFREE We conclude that DNA mismatch repair defects involving hMLH1 and hMSH2 underexpression are extremely rare events in sporadic and familial breast cancer. 14520695 2003