Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913530
rs121913530
KRAS
0.880 GeneticVariation UNIPROT

dbSNP: rs121913530
rs121913530
KRAS
A 0.880 CausalMutation CLINVAR

dbSNP: rs121909071
rs121909071
SLC22A18
T 0.800 CausalMutation CLINVAR

dbSNP: rs34424986
rs34424986
PRKN
A 0.720 CausalMutation CLINVAR

dbSNP: rs104894360
rs104894360
KRAS
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913281
rs121913281
PIK3CA
T 0.700 CausalMutation CLINVAR

dbSNP: rs121917901
rs121917901
ERCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs121917902
rs121917902
ERCC6 ; PGBD3
A 0.700 CausalMutation CLINVAR

dbSNP: rs1324578301
rs1324578301
NTRK2
0.700 GeneticVariation UNIPROT

dbSNP: rs17851045
rs17851045
KRAS
0.700 GeneticVariation UNIPROT

dbSNP: rs180177042
rs180177042
BRAF
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1805076
rs1805076
PPP2R1B
T 0.700 CausalMutation CLINVAR

dbSNP: rs2071460
rs2071460
CSNK2A3 ; GALNT18
0.700 GeneticVariation UNIPROT

dbSNP: rs372594677
rs372594677
EPHA3
0.700 GeneticVariation UNIPROT

dbSNP: rs373227647
rs373227647
ERCC6
C 0.700 CausalMutation CLINVAR

dbSNP: rs376526037
rs376526037
ERCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906660
rs387906660
BRAF
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906661
rs387906661
BRAF
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507466
rs397507466
BRAF
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397516895
rs397516895
BRAF
T 0.700 GeneticVariation CLINVAR

dbSNP: rs540635787
rs540635787
CHEK2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587782705
rs587782705
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs4787050
rs4787050
RBFOX1
0.010 GeneticVariation BEFREE <b>Conclusion:</b> The present study revealed that rs4787050 and rs8045980 in <i>RBFOX1</i> may be meaningful as a novel biomarker for lung cancer susceptibility. 31512508

2019
dbSNP: rs8045980
rs8045980
RBFOX1
0.010 GeneticVariation BEFREE <b>Conclusion:</b> The present study revealed that rs4787050 and rs8045980 in <i>RBFOX1</i> may be meaningful as a novel biomarker for lung cancer susceptibility. 31512508

2019
dbSNP: rs10053847
rs10053847
IL7R
0.010 GeneticVariation BEFREE <i>IL-7R</i> rs10053847 was correlated with a decreased LC risk, while <i>IL-7R</i> rs10213865 was correlated with an elevated lung adenocarcinoma risk, implying these two SNPs might play essential roles in LC risk evaluation. 31354347

2019