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rs9266161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9266161(A;G)
Make rs9266161(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356717
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266161
ebirs9266161
HLIrs9266161
Exacrs9266161
Varsomers9266161
Maprs9266161
PheGenIrs9266161
hapmaprs9266161
1000 genomesrs9266161
hgdprs9266161
ensemblrs9266161
gopubmedrs9266161
geneviewrs9266161
scholarrs9266161
googlers9266161
pharmgkbrs9266161
gwascentralrs9266161
openSNPrs9266161
23andMers9266161
23andMe allrs9266161
SNP Nexus

SNPshotrs9266161
SNPdbers9266161
MSV3drs9266161
GWAS Ctlgrs9266161
Max Magnitude0
ClinVar
Risk rs9266161(C,G;C,G)
Alt rs9266161(C,G;C,G)
Reference rs9266161(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324494A>C; NC_000006.11:g.31324494A>G
CLNSRC
CLNACC