rs4899260
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4899260(C;C) |
Make rs4899260(C;T) |
Make rs4899260(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 68811487 |
is a | snp |
is | mentioned by |
dbSNP | rs4899260 |
dbSNP (classic) | rs4899260 |
ClinGen | rs4899260 |
ebi | rs4899260 |
HLI | rs4899260 |
Exac | rs4899260 |
Gnomad | rs4899260 |
Varsome | rs4899260 |
LitVar | rs4899260 |
Map | rs4899260 |
PheGenI | rs4899260 |
Biobank | rs4899260 |
1000 genomes | rs4899260 |
hgdp | rs4899260 |
ensembl | rs4899260 |
geneview | rs4899260 |
scholar | rs4899260 |
rs4899260 | |
pharmgkb | rs4899260 |
gwascentral | rs4899260 |
openSNP | rs4899260 |
23andMe | rs4899260 |
SNPshot | rs4899260 |
SNPdbe | rs4899260 |
MSV3d | rs4899260 |
GWAS Ctlg | rs4899260 |
GMAF | 0.1988 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 4E-7 |
Odds Ratio | 1.12 [1.07-1.16] |