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rs9266225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9266225(C;C)
Make rs9266225(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357416
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266225
ebirs9266225
HLIrs9266225
Exacrs9266225
Varsomers9266225
Maprs9266225
PheGenIrs9266225
hapmaprs9266225
1000 genomesrs9266225
hgdprs9266225
ensemblrs9266225
gopubmedrs9266225
geneviewrs9266225
scholarrs9266225
googlers9266225
pharmgkbrs9266225
gwascentralrs9266225
openSNPrs9266225
23andMers9266225
23andMe allrs9266225
SNP Nexus

SNPshotrs9266225
SNPdbers9266225
MSV3drs9266225
GWAS Ctlgrs9266225
GMAF0.3921
Max Magnitude0
ClinVar
Risk rs9266225(C;C)
Alt rs9266225(C;C)
Reference rs9266225(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31325193T>C
CLNSRC
CLNACC