Have questions? Visit https://www.reddit.com/r/SNPedia

rs9296068

From SNPedia

Orientationplus
Stabilizedplus
Make rs9296068(G;G)
Make rs9296068(G;T)
Make rs9296068(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position33020918
is asnp
is mentioned by
dbSNPrs9296068
ebirs9296068
HLIrs9296068
Exacrs9296068
Varsomers9296068
Maprs9296068
PheGenIrs9296068
hapmaprs9296068
1000 genomesrs9296068
hgdprs9296068
ensemblrs9296068
gopubmedrs9296068
geneviewrs9296068
scholarrs9296068
googlers9296068
pharmgkbrs9296068
gwascentralrs9296068
openSNPrs9296068
23andMers9296068
23andMe allrs9296068
SNP Nexus

SNPshotrs9296068
SNPdbers9296068
MSV3drs9296068
GWAS Ctlgrs9296068
GMAF0.4518
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 18639552OA-icon.png] 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 23991122OA-icon.png] 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.