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rs9266175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9266175(C;T)
Make rs9266175(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356797
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266175
ebirs9266175
HLIrs9266175
Exacrs9266175
Varsomers9266175
Maprs9266175
PheGenIrs9266175
hapmaprs9266175
1000 genomesrs9266175
hgdprs9266175
ensemblrs9266175
gopubmedrs9266175
geneviewrs9266175
scholarrs9266175
googlers9266175
pharmgkbrs9266175
gwascentralrs9266175
openSNPrs9266175
23andMers9266175
23andMe allrs9266175
SNP Nexus

SNPshotrs9266175
SNPdbers9266175
MSV3drs9266175
GWAS Ctlgrs9266175
GMAF0.03076
Max Magnitude0
ClinVar
Risk rs9266175(T;T)
Alt rs9266175(T;T)
Reference rs9266175(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324574C>T
CLNSRC
CLNACC