Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4987188
rs4987188
MSH2
CUI: C0265325
Disease: Turcot syndrome (disorder)
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