rs7665090
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7665090(A;A) |
| Make rs7665090(A;G) |
| Make rs7665090(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 102630446 |
| Gene | MANBA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7665090 |
| dbSNP (classic) | rs7665090 |
| ClinGen | rs7665090 |
| ebi | rs7665090 |
| HLI | rs7665090 |
| Exac | rs7665090 |
| Gnomad | rs7665090 |
| Varsome | rs7665090 |
| LitVar | rs7665090 |
| Map | rs7665090 |
| PheGenI | rs7665090 |
| Biobank | rs7665090 |
| 1000 genomes | rs7665090 |
| hgdp | rs7665090 |
| ensembl | rs7665090 |
| geneview | rs7665090 |
| scholar | rs7665090 |
| rs7665090 | |
| pharmgkb | rs7665090 |
| gwascentral | rs7665090 |
| openSNP | rs7665090 |
| 23andMe | rs7665090 |
| SNPshot | rs7665090 |
| SNPdbe | rs7665090 |
| MSV3d | rs7665090 |
| GWAS Ctlg | rs7665090 |
| GMAF | 0.4504 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21399635 ]
|
| Trait | |
| Title | Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis |
| Risk Allele | C |
| P-val | 4E-12 |
| Odds Ratio | 1.2600 [1.18-1.34] |
[PMID 23543094] Testing for associations between loci and environmental gradients using latent factor mixed models.
