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rs9266178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9266178(C;T)
Make rs9266178(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356826
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266178
ebirs9266178
HLIrs9266178
Exacrs9266178
Varsomers9266178
Maprs9266178
PheGenIrs9266178
hapmaprs9266178
1000 genomesrs9266178
hgdprs9266178
ensemblrs9266178
gopubmedrs9266178
geneviewrs9266178
scholarrs9266178
googlers9266178
pharmgkbrs9266178
gwascentralrs9266178
openSNPrs9266178
23andMers9266178
23andMe allrs9266178
SNP Nexus

SNPshotrs9266178
SNPdbers9266178
MSV3drs9266178
GWAS Ctlgrs9266178
GMAF0.1685
Max Magnitude0
ClinVar
Risk rs9266178(T;T)
Alt rs9266178(T;T)
Reference rs9266178(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324603C>T
CLNSRC
CLNACC