MSH6, mutS homolog 6, 2956

N. diseases: 296; N. variants: 642
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 MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer. 29345684 2018
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.310 Biomarker disease CLINGEN Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer. 26976419 2016
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.310 GeneticVariation disease BEFREE Association of rare MSH6 variants with familial breast cancer. 19924528 2010
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.310 Biomarker disease CLINGEN No MSH6 germline mutations in breast cancer families with colorectal and/or endometrial cancer. 15805151 2005
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.310 Biomarker disease CLINGEN Exclusion of breast cancer as an integral tumor of hereditary nonpolyposis colorectal cancer. 11861375 2002