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rs9303196

From SNPedia

Orientationplus
Stabilizedplus
Make rs9303196(A;A)
Make rs9303196(A;T)
Make rs9303196(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position6004123
is asnp
is mentioned by
dbSNPrs9303196
ebirs9303196
HLIrs9303196
Exacrs9303196
Varsomers9303196
Maprs9303196
PheGenIrs9303196
hapmaprs9303196
1000 genomesrs9303196
hgdprs9303196
ensemblrs9303196
gopubmedrs9303196
geneviewrs9303196
scholarrs9303196
googlers9303196
pharmgkbrs9303196
gwascentralrs9303196
openSNPrs9303196
23andMers9303196
23andMe allrs9303196
SNP Nexus

SNPshotrs9303196
SNPdbers9303196
MSV3drs9303196
GWAS Ctlgrs9303196
GMAF0.1671
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 20876614]
Trait
Title A Genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population
Risk Allele T
P-val 0.000008
Odds Ratio 1.43 [1.14-1.82]