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rs2181033

From SNPedia

Orientationplus
Stabilizedplus
Make rs2181033(A;A)
Make rs2181033(A;G)
Make rs2181033(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position114935551
is asnp
is mentioned by
dbSNPrs2181033
ebirs2181033
HLIrs2181033
Exacrs2181033
Varsomers2181033
Maprs2181033
PheGenIrs2181033
hapmaprs2181033
1000 genomesrs2181033
hgdprs2181033
ensemblrs2181033
gopubmedrs2181033
geneviewrs2181033
scholarrs2181033
googlers2181033
pharmgkbrs2181033
gwascentralrs2181033
openSNPrs2181033
23andMers2181033
23andMe allrs2181033
SNP Nexus

SNPshotrs2181033
SNPdbers2181033
MSV3drs2181033
GWAS Ctlgrs2181033
GMAF0.3219
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21292647OA-icon.png] Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer - a finding from Texas lung cancer genome-wide association study