rs10903122
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10903122(A;A) |
Make rs10903122(A;G) |
Make rs10903122(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 24977085 |
is a | snp |
is | mentioned by |
dbSNP | rs10903122 |
dbSNP (classic) | rs10903122 |
ClinGen | rs10903122 |
ebi | rs10903122 |
HLI | rs10903122 |
Exac | rs10903122 |
Gnomad | rs10903122 |
Varsome | rs10903122 |
LitVar | rs10903122 |
Map | rs10903122 |
PheGenI | rs10903122 |
Biobank | rs10903122 |
1000 genomes | rs10903122 |
hgdp | rs10903122 |
ensembl | rs10903122 |
geneview | rs10903122 |
scholar | rs10903122 |
rs10903122 | |
pharmgkb | rs10903122 |
gwascentral | rs10903122 |
openSNP | rs10903122 |
23andMe | rs10903122 |
SNPshot | rs10903122 |
SNPdbe | rs10903122 |
MSV3d | rs10903122 |
GWAS Ctlg | rs10903122 |
GMAF | 0.3825 |
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 | |
P-val | 2E-10 |
Odds Ratio | 1.12 [1.09-1.18] |