rs2181033
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2181033(A;A) |
Make rs2181033(A;G) |
Make rs2181033(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 114935551 |
is a | snp |
is | mentioned by |
dbSNP | rs2181033 |
dbSNP (classic) | rs2181033 |
ClinGen | rs2181033 |
ebi | rs2181033 |
HLI | rs2181033 |
Exac | rs2181033 |
Gnomad | rs2181033 |
Varsome | rs2181033 |
LitVar | rs2181033 |
Map | rs2181033 |
PheGenI | rs2181033 |
Biobank | rs2181033 |
1000 genomes | rs2181033 |
hgdp | rs2181033 |
ensembl | rs2181033 |
geneview | rs2181033 |
scholar | rs2181033 |
rs2181033 | |
pharmgkb | rs2181033 |
gwascentral | rs2181033 |
openSNP | rs2181033 |
23andMe | rs2181033 |
SNPshot | rs2181033 |
SNPdbe | rs2181033 |
MSV3d | rs2181033 |
GWAS Ctlg | rs2181033 |
GMAF | 0.3219 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21292647] 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