rs17760268
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs17760268(C;T) |
| Make rs17760268(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 17 |
| Position | 56533930 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17760268 |
| dbSNP (classic) | rs17760268 |
| ClinGen | rs17760268 |
| ebi | rs17760268 |
| HLI | rs17760268 |
| Exac | rs17760268 |
| Gnomad | rs17760268 |
| Varsome | rs17760268 |
| LitVar | rs17760268 |
| Map | rs17760268 |
| PheGenI | rs17760268 |
| Biobank | rs17760268 |
| 1000 genomes | rs17760268 |
| hgdp | rs17760268 |
| ensembl | rs17760268 |
| geneview | rs17760268 |
| scholar | rs17760268 |
| rs17760268 | |
| pharmgkb | rs17760268 |
| gwascentral | rs17760268 |
| openSNP | rs17760268 |
| 23andMe | rs17760268 |
| SNPshot | rs17760268 |
| SNPdbe | rs17760268 |
| MSV3d | rs17760268 |
| GWAS Ctlg | rs17760268 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | C |
| P-val | 4E-6 |
| Odds Ratio | NR NR |
