rs9936833
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9936833(C;C) |
| Make rs9936833(C;T) |
| Make rs9936833(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 86369512 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9936833 |
| dbSNP (classic) | rs9936833 |
| ClinGen | rs9936833 |
| ebi | rs9936833 |
| HLI | rs9936833 |
| Exac | rs9936833 |
| Gnomad | rs9936833 |
| Varsome | rs9936833 |
| LitVar | rs9936833 |
| Map | rs9936833 |
| PheGenI | rs9936833 |
| Biobank | rs9936833 |
| 1000 genomes | rs9936833 |
| hgdp | rs9936833 |
| ensembl | rs9936833 |
| geneview | rs9936833 |
| scholar | rs9936833 |
| rs9936833 | |
| pharmgkb | rs9936833 |
| gwascentral | rs9936833 |
| openSNP | rs9936833 |
| 23andMe | rs9936833 |
| SNPshot | rs9936833 |
| SNPdbe | rs9936833 |
| MSV3d | rs9936833 |
| GWAS Ctlg | rs9936833 |
| GMAF | 0.32 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22961001
] Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus
[PMID 23504527] Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk.
[PMID 25164089] The OSR1 rs12329305 Polymorphism Contributes to the Development of Congenital Malformations in Cases of Stillborn/Neonatal Death
