rs1801155, APC

N. diseases: 42
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 findings support the hypothesis that the I1307K mutation is unique to the Ashkenazi Jews, contributes to tumor predisposition in colorectal cancer, and is unrelated to mismatch repair deficiency. 9869603 1999