rs6672420
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6672420(A;A) |
Make rs6672420(A;T) |
Make rs6672420(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 24964519 |
Gene | LOC105376878, RUNX3 |
is a | snp |
is | mentioned by |
dbSNP | rs6672420 |
dbSNP (classic) | rs6672420 |
ClinGen | rs6672420 |
ebi | rs6672420 |
HLI | rs6672420 |
Exac | rs6672420 |
Gnomad | rs6672420 |
Varsome | rs6672420 |
LitVar | rs6672420 |
Map | rs6672420 |
PheGenI | rs6672420 |
Biobank | rs6672420 |
1000 genomes | rs6672420 |
hgdp | rs6672420 |
ensembl | rs6672420 |
geneview | rs6672420 |
scholar | rs6672420 |
rs6672420 | |
pharmgkb | rs6672420 |
gwascentral | rs6672420 |
openSNP | rs6672420 |
23andMe | rs6672420 |
SNPshot | rs6672420 |
SNPdbe | rs6672420 |
MSV3d | rs6672420 |
GWAS Ctlg | rs6672420 |
GMAF | 0.4545 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 19728008] Significant association of RUNX3 T/A polymorphism at intron 3 (rs760805) with the risk of gastric atrophy in Helicobacter pylori seropositive Japanese