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rs2596497

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs2596497(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354927
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596497
ebirs2596497
HLIrs2596497
Exacrs2596497
Varsomers2596497
Maprs2596497
PheGenIrs2596497
hapmaprs2596497
1000 genomesrs2596497
hgdprs2596497
ensemblrs2596497
gopubmedrs2596497
geneviewrs2596497
scholarrs2596497
googlers2596497
pharmgkbrs2596497
gwascentralrs2596497
openSNPrs2596497
23andMers2596497
23andMe allrs2596497
SNP Nexus

SNPshotrs2596497
SNPdbers2596497
MSV3drs2596497
GWAS Ctlgrs2596497
GMAF0.1538
Max Magnitude0
ClinVar
Risk rs2596497(C;C)
Alt rs2596497(C;C)
Reference rs2596497(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322704A>G
CLNSRC
CLNACC