Have questions? Visit https://www.reddit.com/r/SNPedia

rs9266150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9266150(A;C)
Make rs9266150(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356368
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9266150
ebirs9266150
HLIrs9266150
Exacrs9266150
Varsomers9266150
Maprs9266150
PheGenIrs9266150
hapmaprs9266150
1000 genomesrs9266150
hgdprs9266150
ensemblrs9266150
gopubmedrs9266150
geneviewrs9266150
scholarrs9266150
googlers9266150
pharmgkbrs9266150
gwascentralrs9266150
openSNPrs9266150
23andMers9266150
23andMe allrs9266150
SNP Nexus

SNPshotrs9266150
SNPdbers9266150
MSV3drs9266150
GWAS Ctlgrs9266150
Max Magnitude0
ClinVar
Risk rs9266150(C,G,T;C,G,T)
Alt rs9266150(C,G,T;C,G,T)
Reference rs9266150(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324145A>C; NC_000006.11:g.31324145A>G; NC_000006.11:g.31324145A>T
CLNSRC
CLNACC