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rs9266193

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9266193(C;C)
Make rs9266193(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357011
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266193
ebirs9266193
HLIrs9266193
Exacrs9266193
Varsomers9266193
Maprs9266193
PheGenIrs9266193
hapmaprs9266193
1000 genomesrs9266193
hgdprs9266193
ensemblrs9266193
gopubmedrs9266193
geneviewrs9266193
scholarrs9266193
googlers9266193
pharmgkbrs9266193
gwascentralrs9266193
openSNPrs9266193
23andMers9266193
23andMe allrs9266193
SNP Nexus

SNPshotrs9266193
SNPdbers9266193
MSV3drs9266193
GWAS Ctlgrs9266193
GMAF0.4481
Max Magnitude0
ClinVar
Risk rs9266193(C;C)
Alt rs9266193(C;C)
Reference rs9266193(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324788T>C
CLNSRC
CLNACC