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rs9266184

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9266184(G;G)
Make rs9266184(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356887
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266184
ebirs9266184
HLIrs9266184
Exacrs9266184
Varsomers9266184
Maprs9266184
PheGenIrs9266184
hapmaprs9266184
1000 genomesrs9266184
hgdprs9266184
ensemblrs9266184
gopubmedrs9266184
geneviewrs9266184
scholarrs9266184
googlers9266184
pharmgkbrs9266184
gwascentralrs9266184
openSNPrs9266184
23andMers9266184
23andMe allrs9266184
SNP Nexus

SNPshotrs9266184
SNPdbers9266184
MSV3drs9266184
GWAS Ctlgrs9266184
GMAF0.2103
Max Magnitude0
ClinVar
Risk rs9266184(C,G;C,G)
Alt rs9266184(C,G;C,G)
Reference rs9266184(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324664T>C; NC_000006.11:g.31324664T>G
CLNSRC
CLNACC