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rs2596492

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2596492(C;C)
Make rs2596492(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356934
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596492
ebirs2596492
HLIrs2596492
Exacrs2596492
Varsomers2596492
Maprs2596492
PheGenIrs2596492
hapmaprs2596492
1000 genomesrs2596492
hgdprs2596492
ensemblrs2596492
gopubmedrs2596492
geneviewrs2596492
scholarrs2596492
googlers2596492
pharmgkbrs2596492
gwascentralrs2596492
openSNPrs2596492
23andMers2596492
23andMe allrs2596492
SNP Nexus

SNPshotrs2596492
SNPdbers2596492
MSV3drs2596492
GWAS Ctlgrs2596492
GMAF0.1635
Max Magnitude0
ClinVar
Risk rs2596492(C,G;C,G)
Alt rs2596492(C,G;C,G)
Reference rs2596492(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324711A>C; NC_000006.11:g.31324711A>G
CLNSRC
CLNACC