rs4679904
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4679904(C;C) |
| Make rs4679904(C;T) |
| Make rs4679904(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 160623108 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4679904 |
| dbSNP (classic) | rs4679904 |
| ClinGen | rs4679904 |
| ebi | rs4679904 |
| HLI | rs4679904 |
| Exac | rs4679904 |
| Gnomad | rs4679904 |
| Varsome | rs4679904 |
| LitVar | rs4679904 |
| Map | rs4679904 |
| PheGenI | rs4679904 |
| Biobank | rs4679904 |
| 1000 genomes | rs4679904 |
| hgdp | rs4679904 |
| ensembl | rs4679904 |
| geneview | rs4679904 |
| scholar | rs4679904 |
| rs4679904 | |
| pharmgkb | rs4679904 |
| gwascentral | rs4679904 |
| openSNP | rs4679904 |
| 23andMe | rs4679904 |
| SNPshot | rs4679904 |
| SNPdbe | rs4679904 |
| MSV3d | rs4679904 |
| GWAS Ctlg | rs4679904 |
| GMAF | 0.186 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19458352 ]
|
| Trait | Primary biliary cirrhosis |
| Title | Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants |
| Risk Allele | G |
| P-val | 0.000001 |
| Odds Ratio | 1.38 [1.21-1.57] |
