Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913535
rs121913535
0.710 GeneticVariation BEFREE KRAS mutations were found in 18 (7.2%) patients (15 in adenocarcinoma, 2 in squamous cell carcinoma and one in NSCLC-not otherwise specified), including an uncommon substitution G13C. 24040454

2013

dbSNP: rs121913535
rs121913535
T 0.710 CausalMutation CLINVAR Frequency and distinctive spectrum of KRAS mutations in never smokers with lung adenocarcinoma. 18794081

2008

dbSNP: rs121913535
rs121913535
G 0.710 CausalMutation CLINVAR Frequency and distinctive spectrum of KRAS mutations in never smokers with lung adenocarcinoma. 18794081

2008

dbSNP: rs121913535
rs121913535
A 0.710 CausalMutation CLINVAR Frequency and distinctive spectrum of KRAS mutations in never smokers with lung adenocarcinoma. 18794081

2008

dbSNP: rs121913535
rs121913535
G 0.710 CausalMutation CLINVAR KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib. 15696205

2005

dbSNP: rs121913535
rs121913535
A 0.710 CausalMutation CLINVAR KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib. 15696205

2005

dbSNP: rs121913535
rs121913535
A 0.710 CausalMutation CLINVAR BRAF and RAS mutations in human lung cancer and melanoma. 12460918

2002

dbSNP: rs121913535
rs121913535
G 0.710 CausalMutation CLINVAR BRAF and RAS mutations in human lung cancer and melanoma. 12460918

2002

dbSNP: rs121913535
rs121913535
T 0.710 CausalMutation CLINVAR BRAF and RAS mutations in human lung cancer and melanoma. 12460918

2002