rs12928822
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common on affy axiom data |
| Make rs12928822(C;T) |
| Make rs12928822(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 11310036 |
| Gene | LOC105371082 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12928822 |
| dbSNP (classic) | rs12928822 |
| ClinGen | rs12928822 |
| ebi | rs12928822 |
| HLI | rs12928822 |
| Exac | rs12928822 |
| Gnomad | rs12928822 |
| Varsome | rs12928822 |
| LitVar | rs12928822 |
| Map | rs12928822 |
| PheGenI | rs12928822 |
| Biobank | rs12928822 |
| 1000 genomes | rs12928822 |
| hgdp | rs12928822 |
| ensembl | rs12928822 |
| geneview | rs12928822 |
| scholar | rs12928822 |
| rs12928822 | |
| pharmgkb | rs12928822 |
| gwascentral | rs12928822 |
| openSNP | rs12928822 |
| 23andMe | rs12928822 |
| SNPshot | rs12928822 |
| SNPdbe | rs12928822 |
| MSV3d | rs12928822 |
| GWAS Ctlg | rs12928822 |
| GMAF | 0.09091 |
| 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 | 3E-8 |
| Odds Ratio | 1.16 [1.10-1.22] |
[PMID 19557189] Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
