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rs9266162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9266162(C;C)
Make rs9266162(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356718
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266162
ebirs9266162
HLIrs9266162
Exacrs9266162
Varsomers9266162
Maprs9266162
PheGenIrs9266162
hapmaprs9266162
1000 genomesrs9266162
hgdprs9266162
ensemblrs9266162
gopubmedrs9266162
geneviewrs9266162
scholarrs9266162
googlers9266162
pharmgkbrs9266162
gwascentralrs9266162
openSNPrs9266162
23andMers9266162
23andMe allrs9266162
SNP Nexus

SNPshotrs9266162
SNPdbers9266162
MSV3drs9266162
GWAS Ctlgrs9266162
Max Magnitude0
ClinVar
Risk rs9266162(A,C,T;A,C,T)
Alt rs9266162(A,C,T;A,C,T)
Reference rs9266162(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324495G>A; NC_000006.11:g.31324495G>C; NC_000006.11:g.31324495G>T
CLNSRC
CLNACC