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rs9266197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9266197(A;A)
Make rs9266197(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357053
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266197
ebirs9266197
HLIrs9266197
Exacrs9266197
Varsomers9266197
Maprs9266197
PheGenIrs9266197
hapmaprs9266197
1000 genomesrs9266197
hgdprs9266197
ensemblrs9266197
gopubmedrs9266197
geneviewrs9266197
scholarrs9266197
googlers9266197
pharmgkbrs9266197
gwascentralrs9266197
openSNPrs9266197
23andMers9266197
23andMe allrs9266197
SNP Nexus

SNPshotrs9266197
SNPdbers9266197
MSV3drs9266197
GWAS Ctlgrs9266197
GMAF0.2819
Max Magnitude0
ClinVar
Risk rs9266197(A;A)
Alt rs9266197(A;A)
Reference rs9266197(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324830G>A
CLNSRC
CLNACC