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rs9266198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9266198(C;G)
Make rs9266198(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357070
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266198
ebirs9266198
HLIrs9266198
Exacrs9266198
Varsomers9266198
Maprs9266198
PheGenIrs9266198
hapmaprs9266198
1000 genomesrs9266198
hgdprs9266198
ensemblrs9266198
gopubmedrs9266198
geneviewrs9266198
scholarrs9266198
googlers9266198
pharmgkbrs9266198
gwascentralrs9266198
openSNPrs9266198
23andMers9266198
23andMe allrs9266198
SNP Nexus

SNPshotrs9266198
SNPdbers9266198
MSV3drs9266198
GWAS Ctlgrs9266198
GMAF0.3099
Max Magnitude0
ClinVar
Risk rs9266198(G;G)
Alt rs9266198(G;G)
Reference rs9266198(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324847C>G
CLNSRC
CLNACC