rs2605393
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2605393(G;G) |
Make rs2605393(G;T) |
Make rs2605393(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 36368109 |
is a | snp |
is | mentioned by |
dbSNP | rs2605393 |
dbSNP (classic) | rs2605393 |
ClinGen | rs2605393 |
ebi | rs2605393 |
HLI | rs2605393 |
Exac | rs2605393 |
Gnomad | rs2605393 |
Varsome | rs2605393 |
LitVar | rs2605393 |
Map | rs2605393 |
PheGenI | rs2605393 |
Biobank | rs2605393 |
1000 genomes | rs2605393 |
hgdp | rs2605393 |
ensembl | rs2605393 |
geneview | rs2605393 |
scholar | rs2605393 |
rs2605393 | |
pharmgkb | rs2605393 |
gwascentral | rs2605393 |
openSNP | rs2605393 |
23andMe | rs2605393 |
SNPshot | rs2605393 |
SNPdbe | rs2605393 |
MSV3d | rs2605393 |
GWAS Ctlg | rs2605393 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23936387] |
Trait | Celiac disease |
Title | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
Risk Allele | G |
P-val | 6E-6 |
Odds Ratio | NR NR |