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rs1131279

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(C;C) 0 common in complete genomics
Make rs1131279(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356181
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1131279
ebirs1131279
HLIrs1131279
Exacrs1131279
Varsomers1131279
Maprs1131279
PheGenIrs1131279
hapmaprs1131279
1000 genomesrs1131279
hgdprs1131279
ensemblrs1131279
gopubmedrs1131279
geneviewrs1131279
scholarrs1131279
googlers1131279
pharmgkbrs1131279
gwascentralrs1131279
openSNPrs1131279
23andMers1131279
23andMe allrs1131279
SNP Nexus

SNPshotrs1131279
SNPdbers1131279
MSV3drs1131279
GWAS Ctlgrs1131279
GMAF0.2374
Max Magnitude0
ClinVar
Risk rs1131279(C,T;C,T)
Alt rs1131279(C,T;C,T)
Reference rs1131279(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323958T>A; NC_000006.11:g.31323958T>G
CLNSRC
CLNACC