rs13010713
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13010713(A;A) |
Make rs13010713(A;G) |
Make rs13010713(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 181131318 |
Gene | LINC01934 |
is a | snp |
is | mentioned by |
dbSNP | rs13010713 |
dbSNP (classic) | rs13010713 |
ClinGen | rs13010713 |
ebi | rs13010713 |
HLI | rs13010713 |
Exac | rs13010713 |
Gnomad | rs13010713 |
Varsome | rs13010713 |
LitVar | rs13010713 |
Map | rs13010713 |
PheGenI | rs13010713 |
Biobank | rs13010713 |
1000 genomes | rs13010713 |
hgdp | rs13010713 |
ensembl | rs13010713 |
geneview | rs13010713 |
scholar | rs13010713 |
rs13010713 | |
pharmgkb | rs13010713 |
gwascentral | rs13010713 |
openSNP | rs13010713 |
23andMe | rs13010713 |
SNPshot | rs13010713 |
SNPdbe | rs13010713 |
MSV3d | rs13010713 |
GWAS Ctlg | rs13010713 |
GMAF | 0.4472 |
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 | G |
P-val | 5E-11 |
Odds Ratio | 1.13 [1.09-1.18] |