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rs9266194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9266194(A;G)
Make rs9266194(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357013
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266194
ebirs9266194
HLIrs9266194
Exacrs9266194
Varsomers9266194
Maprs9266194
PheGenIrs9266194
hapmaprs9266194
1000 genomesrs9266194
hgdprs9266194
ensemblrs9266194
gopubmedrs9266194
geneviewrs9266194
scholarrs9266194
googlers9266194
pharmgkbrs9266194
gwascentralrs9266194
openSNPrs9266194
23andMers9266194
23andMe allrs9266194
SNP Nexus

SNPshotrs9266194
SNPdbers9266194
MSV3drs9266194
GWAS Ctlgrs9266194
GMAF0.449
Max Magnitude0
ClinVar
Risk rs9266194(G;G)
Alt rs9266194(G;G)
Reference rs9266194(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324790A>G
CLNSRC
CLNACC