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rs2596496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2596496(C;C)
Make rs2596496(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355005
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596496
ebirs2596496
HLIrs2596496
Exacrs2596496
Varsomers2596496
Maprs2596496
PheGenIrs2596496
hapmaprs2596496
1000 genomesrs2596496
hgdprs2596496
ensemblrs2596496
gopubmedrs2596496
geneviewrs2596496
scholarrs2596496
googlers2596496
pharmgkbrs2596496
gwascentralrs2596496
openSNPrs2596496
23andMers2596496
23andMe allrs2596496
SNP Nexus

SNPshotrs2596496
SNPdbers2596496
MSV3drs2596496
GWAS Ctlgrs2596496
GMAF0.2925
Max Magnitude0
ClinVar
Risk rs2596496(C;C)
Alt rs2596496(C;C)
Reference rs2596496(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322782C>G
CLNSRC
CLNACC