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rs9266207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9266207(C;T)
Make rs9266207(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357176
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266207
ebirs9266207
HLIrs9266207
Exacrs9266207
Varsomers9266207
Maprs9266207
PheGenIrs9266207
hapmaprs9266207
1000 genomesrs9266207
hgdprs9266207
ensemblrs9266207
gopubmedrs9266207
geneviewrs9266207
scholarrs9266207
googlers9266207
pharmgkbrs9266207
gwascentralrs9266207
openSNPrs9266207
23andMers9266207
23andMe allrs9266207
SNP Nexus

SNPshotrs9266207
SNPdbers9266207
MSV3drs9266207
GWAS Ctlgrs9266207
GMAF0.2718
Max Magnitude0
ClinVar
Risk rs9266207(T;T)
Alt rs9266207(T;T)
Reference rs9266207(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324953C>T
CLNSRC
CLNACC