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rs9266141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9266141(C;G)
Make rs9266141(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356246
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266141
ebirs9266141
HLIrs9266141
Exacrs9266141
Varsomers9266141
Maprs9266141
PheGenIrs9266141
hapmaprs9266141
1000 genomesrs9266141
hgdprs9266141
ensemblrs9266141
gopubmedrs9266141
geneviewrs9266141
scholarrs9266141
googlers9266141
pharmgkbrs9266141
gwascentralrs9266141
openSNPrs9266141
23andMers9266141
23andMe allrs9266141
SNP Nexus

SNPshotrs9266141
SNPdbers9266141
MSV3drs9266141
GWAS Ctlgrs9266141
Max Magnitude0
ClinVar
Risk rs9266141(G,T;G,T)
Alt rs9266141(G,T;G,T)
Reference rs9266141(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324023C>G; NC_000006.11:g.31324023C>T
CLNSRC
CLNACC