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

rs2596495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2596495(C;G)
Make rs2596495(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355639
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2596495
ebirs2596495
HLIrs2596495
Exacrs2596495
Varsomers2596495
Maprs2596495
PheGenIrs2596495
hapmaprs2596495
1000 genomesrs2596495
hgdprs2596495
ensemblrs2596495
gopubmedrs2596495
geneviewrs2596495
scholarrs2596495
googlers2596495
pharmgkbrs2596495
gwascentralrs2596495
openSNPrs2596495
23andMers2596495
23andMe allrs2596495
SNP Nexus

SNPshotrs2596495
SNPdbers2596495
MSV3drs2596495
GWAS Ctlgrs2596495
GMAF0.07117
Max Magnitude0
ClinVar
Risk rs2596495(G;G)
Alt rs2596495(G;G)
Reference rs2596495(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323416G>C
CLNSRC
CLNACC