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rs2596494

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2596494(C;C)
Make rs2596494(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356061
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596494
ebirs2596494
HLIrs2596494
Exacrs2596494
Varsomers2596494
Maprs2596494
PheGenIrs2596494
hapmaprs2596494
1000 genomesrs2596494
hgdprs2596494
ensemblrs2596494
gopubmedrs2596494
geneviewrs2596494
scholarrs2596494
googlers2596494
pharmgkbrs2596494
gwascentralrs2596494
openSNPrs2596494
23andMers2596494
23andMe allrs2596494
SNP Nexus

SNPshotrs2596494
SNPdbers2596494
MSV3drs2596494
GWAS Ctlgrs2596494
GMAF0.1561
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs2596494(C;C)
Alt rs2596494(C;C)
Reference rs2596494(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323838C>G
CLNSRC
CLNACC