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rs4081560

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs4081560(C;T)
Make rs4081560(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355790
GeneHLA-B
is asnp
is mentioned by
dbSNPrs4081560
ebirs4081560
HLIrs4081560
Exacrs4081560
Varsomers4081560
Maprs4081560
PheGenIrs4081560
hapmaprs4081560
1000 genomesrs4081560
hgdprs4081560
ensemblrs4081560
gopubmedrs4081560
geneviewrs4081560
scholarrs4081560
googlers4081560
pharmgkbrs4081560
gwascentralrs4081560
openSNPrs4081560
23andMers4081560
23andMe allrs4081560
SNP Nexus

SNPshotrs4081560
SNPdbers4081560
MSV3drs4081560
GWAS Ctlgrs4081560
GMAF0.1093
Max Magnitude0
ClinVar
Risk rs4081560(T;T)
Alt rs4081560(T;T)
Reference rs4081560(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323567G>A
CLNSRC
CLNACC