rs3812863
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3812863(A;A) |
| Make rs3812863(A;G) |
| Make rs3812863(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 27971131 |
| Gene | CDX2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3812863 |
| dbSNP (classic) | rs3812863 |
| ClinGen | rs3812863 |
| ebi | rs3812863 |
| HLI | rs3812863 |
| Exac | rs3812863 |
| Gnomad | rs3812863 |
| Varsome | rs3812863 |
| LitVar | rs3812863 |
| Map | rs3812863 |
| PheGenI | rs3812863 |
| Biobank | rs3812863 |
| 1000 genomes | rs3812863 |
| hgdp | rs3812863 |
| ensembl | rs3812863 |
| geneview | rs3812863 |
| scholar | rs3812863 |
| rs3812863 | |
| pharmgkb | rs3812863 |
| gwascentral | rs3812863 |
| openSNP | rs3812863 |
| 23andMe | rs3812863 |
| SNPshot | rs3812863 |
| SNPdbe | rs3812863 |
| MSV3d | rs3812863 |
| GWAS Ctlg | rs3812863 |
| GMAF | 0.4348 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23918153
] Single nucleotide polymorphisms of caudal type homeobox 1 and 2 are associated with Barrett's esophagus
