rs2926702
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2926702(A;A) |
Make rs2926702(A;G) |
Make rs2926702(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 70255759 |
Gene | NCOA2 |
is a | snp |
is | mentioned by |
dbSNP | rs2926702 |
dbSNP (classic) | rs2926702 |
ClinGen | rs2926702 |
ebi | rs2926702 |
HLI | rs2926702 |
Exac | rs2926702 |
Gnomad | rs2926702 |
Varsome | rs2926702 |
LitVar | rs2926702 |
Map | rs2926702 |
PheGenI | rs2926702 |
Biobank | rs2926702 |
1000 genomes | rs2926702 |
hgdp | rs2926702 |
ensembl | rs2926702 |
geneview | rs2926702 |
scholar | rs2926702 |
rs2926702 | |
pharmgkb | rs2926702 |
gwascentral | rs2926702 |
openSNP | rs2926702 |
23andMe | rs2926702 |
SNPshot | rs2926702 |
SNPdbe | rs2926702 |
MSV3d | rs2926702 |
GWAS Ctlg | rs2926702 |
GMAF | 0.1887 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23144319] |
Trait | Non-small cell lung cancer |
Title | Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study. |
Risk Allele | T |
P-val | 7E-6 |
Odds Ratio | NR NR |