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rs2596493

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2596493(G;G)
Make rs2596493(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356168
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596493
ebirs2596493
HLIrs2596493
Exacrs2596493
Varsomers2596493
Maprs2596493
PheGenIrs2596493
hapmaprs2596493
1000 genomesrs2596493
hgdprs2596493
ensemblrs2596493
gopubmedrs2596493
geneviewrs2596493
scholarrs2596493
googlers2596493
pharmgkbrs2596493
gwascentralrs2596493
openSNPrs2596493
23andMers2596493
23andMe allrs2596493
SNP Nexus

SNPshotrs2596493
SNPdbers2596493
MSV3drs2596493
GWAS Ctlgrs2596493
GMAF0.219
Max Magnitude0
ClinVar
Risk rs2596493(A,C,G;A,C,G)
Alt rs2596493(A,C,G;A,C,G)
Reference rs2596493(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323945A>C; NC_000006.11:g.31323945A>G; NC_000006.11:g.31323945A>T
CLNSRC
CLNACC