rs157640
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs157640(G;G) |
Make rs157640(G;T) |
Make rs157640(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 20 |
Position | 54798000 |
is a | snp |
is | mentioned by |
dbSNP | rs157640 |
dbSNP (classic) | rs157640 |
ClinGen | rs157640 |
ebi | rs157640 |
HLI | rs157640 |
Exac | rs157640 |
Gnomad | rs157640 |
Varsome | rs157640 |
LitVar | rs157640 |
Map | rs157640 |
PheGenI | rs157640 |
Biobank | rs157640 |
1000 genomes | rs157640 |
hgdp | rs157640 |
ensembl | rs157640 |
geneview | rs157640 |
scholar | rs157640 |
rs157640 | |
pharmgkb | rs157640 |
gwascentral | rs157640 |
openSNP | rs157640 |
23andMe | rs157640 |
SNPshot | rs157640 |
SNPdbe | rs157640 |
MSV3d | rs157640 |
GWAS Ctlg | rs157640 |
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 | 5E-6 |
Odds Ratio | NR NR |