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rs9266195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9266195(G;T)
Make rs9266195(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357043
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266195
ebirs9266195
HLIrs9266195
Exacrs9266195
Varsomers9266195
Maprs9266195
PheGenIrs9266195
hapmaprs9266195
1000 genomesrs9266195
hgdprs9266195
ensemblrs9266195
gopubmedrs9266195
geneviewrs9266195
scholarrs9266195
googlers9266195
pharmgkbrs9266195
gwascentralrs9266195
openSNPrs9266195
23andMers9266195
23andMe allrs9266195
SNP Nexus

SNPshotrs9266195
SNPdbers9266195
MSV3drs9266195
GWAS Ctlgrs9266195
GMAF0.07759
Max Magnitude0
ClinVar
Risk rs9266195(T;T)
Alt rs9266195(T;T)
Reference rs9266195(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324820G>T
CLNSRC
CLNACC