rs12901001
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12901001(A;A) |
| Make rs12901001(A;G) |
| Make rs12901001(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 86316245 |
| Gene | AGBL1, AGBL1-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12901001 |
| dbSNP (classic) | rs12901001 |
| ClinGen | rs12901001 |
| ebi | rs12901001 |
| HLI | rs12901001 |
| Exac | rs12901001 |
| Gnomad | rs12901001 |
| Varsome | rs12901001 |
| LitVar | rs12901001 |
| Map | rs12901001 |
| PheGenI | rs12901001 |
| Biobank | rs12901001 |
| 1000 genomes | rs12901001 |
| hgdp | rs12901001 |
| ensembl | rs12901001 |
| geneview | rs12901001 |
| scholar | rs12901001 |
| rs12901001 | |
| pharmgkb | rs12901001 |
| gwascentral | rs12901001 |
| openSNP | rs12901001 |
| 23andMe | rs12901001 |
| SNPshot | rs12901001 |
| SNPdbe | rs12901001 |
| MSV3d | rs12901001 |
| GWAS Ctlg | rs12901001 |
| GMAF | 0.461 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22961001 ]
|
| Trait | Barrett's esophagus |
| Title | Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. |
| Risk Allele | |
| P-val | 6E-6 |
| Odds Ratio | .15 [0.091-0.209] unit increase |
