Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519847
rs1057519847
0.030 GeneticVariation BEFREE We report three cases that were definitively diagnosed as LM from NSCLC with a mutation of epidermal growth factor receptor (<i>EGFR</i>) L858R. 31571928

2019

dbSNP: rs1057519847
rs1057519847
0.030 GeneticVariation BEFREE In particular, the primary mutation, L858R, potentially predicts a higher risk of LM compared with deletion of exon 19. 30642536

2019

dbSNP: rs1057519847
rs1057519847
0.030 GeneticVariation BEFREE We have recently identified an EGFR mutation E884K, in combination with L858R, in a patient with advanced lung cancer who progressed on erlotinib maintenance therapy, and subsequently had leptomeningeal metastases that responded to gefitinib. 19015641

2009