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rs9266217

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9266217(A;G)
Make rs9266217(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357315
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266217
ebirs9266217
HLIrs9266217
Exacrs9266217
Varsomers9266217
Maprs9266217
PheGenIrs9266217
hapmaprs9266217
1000 genomesrs9266217
hgdprs9266217
ensemblrs9266217
gopubmedrs9266217
geneviewrs9266217
scholarrs9266217
googlers9266217
pharmgkbrs9266217
gwascentralrs9266217
openSNPrs9266217
23andMers9266217
23andMe allrs9266217
SNP Nexus

SNPshotrs9266217
SNPdbers9266217
MSV3drs9266217
GWAS Ctlgrs9266217
GMAF0.2452
Max Magnitude0
ClinVar
Risk rs9266217(G;G)
Alt rs9266217(G;G)
Reference rs9266217(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31325092A>G
CLNSRC
CLNACC