rs2157453
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2157453(A;A) |
Make rs2157453(A;G) |
Make rs2157453(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 172894808 |
is a | snp |
is | mentioned by |
dbSNP | rs2157453 |
dbSNP (classic) | rs2157453 |
ClinGen | rs2157453 |
ebi | rs2157453 |
HLI | rs2157453 |
Exac | rs2157453 |
Gnomad | rs2157453 |
Varsome | rs2157453 |
LitVar | rs2157453 |
Map | rs2157453 |
PheGenI | rs2157453 |
Biobank | rs2157453 |
1000 genomes | rs2157453 |
hgdp | rs2157453 |
ensembl | rs2157453 |
geneview | rs2157453 |
scholar | rs2157453 |
rs2157453 | |
pharmgkb | rs2157453 |
gwascentral | rs2157453 |
openSNP | rs2157453 |
23andMe | rs2157453 |
SNPshot | rs2157453 |
SNPdbe | rs2157453 |
MSV3d | rs2157453 |
GWAS Ctlg | rs2157453 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24999842![]() |
Trait | Celiac disease |
Title | Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. |
Risk Allele | |
P-val | 8E-7 |
Odds Ratio | 1.29 [1.17–1.42] |