rs859637
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs859637(A;A) |
Make rs859637(A;G) |
Make rs859637(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 172741860 |
is a | snp |
is | mentioned by |
dbSNP | rs859637 |
dbSNP (classic) | rs859637 |
ClinGen | rs859637 |
ebi | rs859637 |
HLI | rs859637 |
Exac | rs859637 |
Gnomad | rs859637 |
Varsome | rs859637 |
LitVar | rs859637 |
Map | rs859637 |
PheGenI | rs859637 |
Biobank | rs859637 |
1000 genomes | rs859637 |
hgdp | rs859637 |
ensembl | rs859637 |
geneview | rs859637 |
scholar | rs859637 |
rs859637 | |
pharmgkb | rs859637 |
gwascentral | rs859637 |
openSNP | rs859637 |
23andMe | rs859637 |
SNPshot | rs859637 |
SNPdbe | rs859637 |
MSV3d | rs859637 |
GWAS Ctlg | rs859637 |
GMAF | 0.4394 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20190752] |
Trait | Celiac disease |
Title | Multiple common variants for celiac disease influencing immune gene expression |
Risk Allele | A |
P-val | 0.000002 |
Odds Ratio | 1.10 [1.06-1.14] |