Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17851045
rs17851045
0.720 GeneticVariation BEFREE In order to rigorously analyze the amount of cfDNA needed, we constructed 72 athymic nude mice xenografted with NCI-H1975 (harboring a EGFR T790M mutation) or NCI-H460 (harboring a KRAS Q61H mutation) human NSCLC. 29497175

2018

dbSNP: rs17851045
rs17851045
0.720 GeneticVariation BEFREE The present studies demonstrate that silencing MUC1-C in A549/KRAS(G12S) and H460/KRAS(Q61H) NSCLC cells is associated with downregulation of AKT signaling and inhibition of growth. 25245423

2014

dbSNP: rs17851045
rs17851045
G 0.720 CausalMutation CLINVAR Frequency and distinctive spectrum of KRAS mutations in never smokers with lung adenocarcinoma. 18794081

2008

dbSNP: rs17851045
rs17851045
A 0.720 CausalMutation CLINVAR Frequency and distinctive spectrum of KRAS mutations in never smokers with lung adenocarcinoma. 18794081

2008

dbSNP: rs17851045
rs17851045
A 0.720 CausalMutation CLINVAR KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib. 15696205

2005

dbSNP: rs17851045
rs17851045
G 0.720 CausalMutation CLINVAR KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib. 15696205

2005

dbSNP: rs17851045
rs17851045
G 0.720 CausalMutation CLINVAR BRAF and RAS mutations in human lung cancer and melanoma. 12460918

2002

dbSNP: rs17851045
rs17851045
A 0.720 CausalMutation CLINVAR BRAF and RAS mutations in human lung cancer and melanoma. 12460918

2002