rs758272654, GNAS

N. diseases: 50
Disease: Esophageal Neoplasms ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
0.030 GeneticVariation BEFREE The aim of the present study was to determine if the single-nucleotide polymorphism GNAS T393C can be used for treatment stratification in esophageal cancer patients. 24986238 2014
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
0.030 GeneticVariation BEFREE Determination of T393C-SNP preoperatively will allow allocation of EC patients into different risk profiles which may help to stratify patients eligible for neoadjuvant and or adjuvant therapy. 21340746 2011
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
0.030 GeneticVariation BEFREE The results support the role of the T393C polymorphism as a predictive molecular marker for tumor response to cisplatin/5-FU-based radiochemotherapy in esophageal cancer. 19274060 2009