rs4987188, MSH2

N. diseases: 11
Disease: Turcot syndrome (disorder) ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.010 GeneticVariation BEFREE Our data demonstrate that MSH2 N127S and G322D per se are not sufficient to trigger MMR deficiency. 18470917 2008