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rs9266218

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9266218(A;G)
Make rs9266218(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357338
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266218
ebirs9266218
HLIrs9266218
Exacrs9266218
Varsomers9266218
Maprs9266218
PheGenIrs9266218
hapmaprs9266218
1000 genomesrs9266218
hgdprs9266218
ensemblrs9266218
gopubmedrs9266218
geneviewrs9266218
scholarrs9266218
googlers9266218
pharmgkbrs9266218
gwascentralrs9266218
openSNPrs9266218
23andMers9266218
23andMe allrs9266218
SNP Nexus

SNPshotrs9266218
SNPdbers9266218
MSV3drs9266218
GWAS Ctlgrs9266218
GMAF0.3425
Max Magnitude0
ClinVar
Risk rs9266218(G;G)
Alt rs9266218(G;G)
Reference rs9266218(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31325115A>G
CLNSRC
CLNACC