rs267607911, MSH2

N. diseases: 8
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
0.010 GeneticVariation BEFREE We report on an ovarian cancer patient who carries a germline MSH2 c.1A>C variant which alters the translation initiation codon. 21837758 2012