rs2236852
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2236852(A;A) |
Make rs2236852(A;G) |
Make rs2236852(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 24917276 |
Gene | RUNX3 |
is a | snp |
is | mentioned by |
dbSNP | rs2236852 |
dbSNP (classic) | rs2236852 |
ClinGen | rs2236852 |
ebi | rs2236852 |
HLI | rs2236852 |
Exac | rs2236852 |
Gnomad | rs2236852 |
Varsome | rs2236852 |
LitVar | rs2236852 |
Map | rs2236852 |
PheGenI | rs2236852 |
Biobank | rs2236852 |
1000 genomes | rs2236852 |
hgdp | rs2236852 |
ensembl | rs2236852 |
geneview | rs2236852 |
scholar | rs2236852 |
rs2236852 | |
pharmgkb | rs2236852 |
gwascentral | rs2236852 |
openSNP | rs2236852 |
23andMe | rs2236852 |
SNPshot | rs2236852 |
SNPdbe | rs2236852 |
MSV3d | rs2236852 |
GWAS Ctlg | rs2236852 |
GMAF | 0.4793 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19552756] Genetic variants in the Runt-related transcription factor 3 gene contribute to gastric cancer risk in a Chinese population
[PMID 18684727] Genetic variants in RUNX3 and risk of bladder cancer: a haplotype-based analysis.