rs17035378
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17035378(C;C) |
| Make rs17035378(C;T) |
| Make rs17035378(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 68371823 |
| Gene | LOC101927723, PLEK |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17035378 |
| dbSNP (classic) | rs17035378 |
| ClinGen | rs17035378 |
| ebi | rs17035378 |
| HLI | rs17035378 |
| Exac | rs17035378 |
| Gnomad | rs17035378 |
| Varsome | rs17035378 |
| LitVar | rs17035378 |
| Map | rs17035378 |
| PheGenI | rs17035378 |
| Biobank | rs17035378 |
| 1000 genomes | rs17035378 |
| hgdp | rs17035378 |
| ensembl | rs17035378 |
| geneview | rs17035378 |
| scholar | rs17035378 |
| rs17035378 | |
| pharmgkb | rs17035378 |
| gwascentral | rs17035378 |
| openSNP | rs17035378 |
| 23andMe | rs17035378 |
| SNPshot | rs17035378 |
| SNPdbe | rs17035378 |
| MSV3d | rs17035378 |
| GWAS Ctlg | rs17035378 |
| GMAF | 0.4421 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752 ]
|
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | |
| P-val | 8E-9 |
| Odds Ratio | 1.14 [1.09-1.19] |
