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rs2596490

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2596490(C;G)
Make rs2596490(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357219
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596490
ebirs2596490
HLIrs2596490
Exacrs2596490
Varsomers2596490
Maprs2596490
PheGenIrs2596490
hapmaprs2596490
1000 genomesrs2596490
hgdprs2596490
ensemblrs2596490
gopubmedrs2596490
geneviewrs2596490
scholarrs2596490
googlers2596490
pharmgkbrs2596490
gwascentralrs2596490
openSNPrs2596490
23andMers2596490
23andMe allrs2596490
SNP Nexus

SNPshotrs2596490
SNPdbers2596490
MSV3drs2596490
GWAS Ctlgrs2596490
GMAF0.1653
Max Magnitude0
ClinVar
Risk rs2596490(G,T;G,T)
Alt rs2596490(G,T;G,T)
Reference rs2596490(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324996G>A; NC_000006.11:g.31324996G>C
CLNSRC
CLNACC