Have questions? Visit https://www.reddit.com/r/SNPedia

rs2596498

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2596498(A;G)
Make rs2596498(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354911
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596498
ebirs2596498
HLIrs2596498
Exacrs2596498
Varsomers2596498
Maprs2596498
PheGenIrs2596498
hapmaprs2596498
1000 genomesrs2596498
hgdprs2596498
ensemblrs2596498
gopubmedrs2596498
geneviewrs2596498
scholarrs2596498
googlers2596498
pharmgkbrs2596498
gwascentralrs2596498
openSNPrs2596498
23andMers2596498
23andMe allrs2596498
SNP Nexus

SNPshotrs2596498
SNPdbers2596498
MSV3drs2596498
GWAS Ctlgrs2596498
GMAF0.2163
Max Magnitude0
ClinVar
Risk rs2596498(G;G)
Alt rs2596498(G;G)
Reference rs2596498(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322688T>C
CLNSRC
CLNACC