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] |
