rs9276982
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9276982(A;A) |
Make rs9276982(A;G) |
Make rs9276982(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 6 |
Position | 33010438 |
Gene | HLA-DOA |
is a | snp |
is | mentioned by |
dbSNP | rs9276982 |
dbSNP (classic) | rs9276982 |
ClinGen | rs9276982 |
ebi | rs9276982 |
HLI | rs9276982 |
Exac | rs9276982 |
Gnomad | rs9276982 |
Varsome | rs9276982 |
LitVar | rs9276982 |
Map | rs9276982 |
PheGenI | rs9276982 |
Biobank | rs9276982 |
1000 genomes | rs9276982 |
hgdp | rs9276982 |
ensembl | rs9276982 |
geneview | rs9276982 |
scholar | rs9276982 |
rs9276982 | |
pharmgkb | rs9276982 |
gwascentral | rs9276982 |
openSNP | rs9276982 |
23andMe | rs9276982 |
SNPshot | rs9276982 |
SNPdbe | rs9276982 |
MSV3d | rs9276982 |
GWAS Ctlg | rs9276982 |
Max Magnitude | 0 |
[PMID 30083439] Single nucleotide polymorphisms within HLA region are associated with disease relapse for patients with unrelated cord blood transplantation.