rs5979785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5979785(C;C) |
| Make rs5979785(C;T) |
| Make rs5979785(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 12953405 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5979785 |
| dbSNP (classic) | rs5979785 |
| ClinGen | rs5979785 |
| ebi | rs5979785 |
| HLI | rs5979785 |
| Exac | rs5979785 |
| Gnomad | rs5979785 |
| Varsome | rs5979785 |
| LitVar | rs5979785 |
| Map | rs5979785 |
| PheGenI | rs5979785 |
| Biobank | rs5979785 |
| 1000 genomes | rs5979785 |
| hgdp | rs5979785 |
| ensembl | rs5979785 |
| geneview | rs5979785 |
| scholar | rs5979785 |
| rs5979785 | |
| pharmgkb | rs5979785 |
| gwascentral | rs5979785 |
| openSNP | rs5979785 |
| 23andMe | rs5979785 |
| SNPshot | rs5979785 |
| SNPdbe | rs5979785 |
| MSV3d | rs5979785 |
| GWAS Ctlg | rs5979785 |
| GMAF | 0.4069 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19956107
] Follow-up of 1715 SNPs from the Wellcome Trust Case Control Consortium genome-wide association study in type I diabetes families
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752]
|
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | |
| P-val | 6E-8 |
| Odds Ratio | 1.14 [1.09-1.19] |
[PMID 19956109] The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.
