rs11249206
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11249206(C;C) |
Make rs11249206(C;T) |
Make rs11249206(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 24951491 |
Gene | LOC105376878, RUNX3 |
is a | snp |
is | mentioned by |
dbSNP | rs11249206 |
dbSNP (classic) | rs11249206 |
ClinGen | rs11249206 |
ebi | rs11249206 |
HLI | rs11249206 |
Exac | rs11249206 |
Gnomad | rs11249206 |
Varsome | rs11249206 |
LitVar | rs11249206 |
Map | rs11249206 |
PheGenI | rs11249206 |
Biobank | rs11249206 |
1000 genomes | rs11249206 |
hgdp | rs11249206 |
ensembl | rs11249206 |
geneview | rs11249206 |
scholar | rs11249206 |
rs11249206 | |
pharmgkb | rs11249206 |
gwascentral | rs11249206 |
openSNP | rs11249206 |
23andMe | rs11249206 |
SNPshot | rs11249206 |
SNPdbe | rs11249206 |
MSV3d | rs11249206 |
GWAS Ctlg | rs11249206 |
GMAF | 0.4747 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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.