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rs9266183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9266183(C;C)
Make rs9266183(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356870
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266183
ebirs9266183
HLIrs9266183
Exacrs9266183
Varsomers9266183
Maprs9266183
PheGenIrs9266183
hapmaprs9266183
1000 genomesrs9266183
hgdprs9266183
ensemblrs9266183
gopubmedrs9266183
geneviewrs9266183
scholarrs9266183
googlers9266183
pharmgkbrs9266183
gwascentralrs9266183
openSNPrs9266183
23andMers9266183
23andMe allrs9266183
SNP Nexus

SNPshotrs9266183
SNPdbers9266183
MSV3drs9266183
GWAS Ctlgrs9266183
GMAF0.03352
Max Magnitude0
ClinVar
Risk rs9266183(C;C)
Alt rs9266183(C;C)
Reference rs9266183(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324647T>C
CLNSRC
CLNACC