rs9296068
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9296068(G;G) |
| Make rs9296068(G;T) |
| Make rs9296068(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 33020918 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9296068 |
| dbSNP (classic) | rs9296068 |
| ClinGen | rs9296068 |
| ebi | rs9296068 |
| HLI | rs9296068 |
| Exac | rs9296068 |
| Gnomad | rs9296068 |
| Varsome | rs9296068 |
| LitVar | rs9296068 |
| Map | rs9296068 |
| PheGenI | rs9296068 |
| Biobank | rs9296068 |
| 1000 genomes | rs9296068 |
| hgdp | rs9296068 |
| ensembl | rs9296068 |
| geneview | rs9296068 |
| scholar | rs9296068 |
| rs9296068 | |
| pharmgkb | rs9296068 |
| gwascentral | rs9296068 |
| openSNP | rs9296068 |
| 23andMe | rs9296068 |
| SNPshot | rs9296068 |
| SNPdbe | rs9296068 |
| MSV3d | rs9296068 |
| GWAS Ctlg | rs9296068 |
| GMAF | 0.4518 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18639552
] rs9296068 significantly different (P = .018) in parent-to-child transmission between outcome groups. The minor allele of the SNP rs9296068 is significantly associated with liver transplantation rejection and with enhanced B-lymphocyte participation in rejection, likely because of a dysfunctional HLA-DOA gene product.
[PMID 23991122] SNP Association Mapping across the Extended Major Histocompatibility Complex and Risk of B-Cell Precursor Acute Lymphoblastic Leukemia in Children
[PMID 26663361] Enhanced B Cell Alloantigen Presentation and Its Epigenetic Dysregulation in Liver Transplant Rejection.
