rs1912785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1912785(A;A) |
| Make rs1912785(A;G) |
| Make rs1912785(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 146684384 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1912785 |
| dbSNP (classic) | rs1912785 |
| ClinGen | rs1912785 |
| ebi | rs1912785 |
| HLI | rs1912785 |
| Exac | rs1912785 |
| Gnomad | rs1912785 |
| Varsome | rs1912785 |
| LitVar | rs1912785 |
| Map | rs1912785 |
| PheGenI | rs1912785 |
| Biobank | rs1912785 |
| 1000 genomes | rs1912785 |
| hgdp | rs1912785 |
| ensembl | rs1912785 |
| geneview | rs1912785 |
| scholar | rs1912785 |
| rs1912785 | |
| pharmgkb | rs1912785 |
| gwascentral | rs1912785 |
| openSNP | rs1912785 |
| 23andMe | rs1912785 |
| SNPshot | rs1912785 |
| SNPdbe | rs1912785 |
| MSV3d | rs1912785 |
| GWAS Ctlg | rs1912785 |
| GMAF | 0.4669 |
| 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 | 8E-6 |
| Odds Ratio | .15 [0.091-0.209] unit decrease |
