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rs9266196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9266196(C;C)
Make rs9266196(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357052
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266196
ebirs9266196
HLIrs9266196
Exacrs9266196
Varsomers9266196
Maprs9266196
PheGenIrs9266196
hapmaprs9266196
1000 genomesrs9266196
hgdprs9266196
ensemblrs9266196
gopubmedrs9266196
geneviewrs9266196
scholarrs9266196
googlers9266196
pharmgkbrs9266196
gwascentralrs9266196
openSNPrs9266196
23andMers9266196
23andMe allrs9266196
SNP Nexus

SNPshotrs9266196
SNPdbers9266196
MSV3drs9266196
GWAS Ctlgrs9266196
GMAF0.2883
Max Magnitude0
ClinVar
Risk rs9266196(C,T;C,T)
Alt rs9266196(C,T;C,T)
Reference rs9266196(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324829G>C; NC_000006.11:g.31324829G>T
CLNSRC
CLNACC