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

rs4081559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4081559(A;A)
Make rs4081559(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355900
GeneHLA-B
is asnp
is mentioned by
dbSNPrs4081559
ebirs4081559
HLIrs4081559
Exacrs4081559
Varsomers4081559
Maprs4081559
PheGenIrs4081559
hapmaprs4081559
1000 genomesrs4081559
hgdprs4081559
ensemblrs4081559
gopubmedrs4081559
geneviewrs4081559
scholarrs4081559
googlers4081559
pharmgkbrs4081559
gwascentralrs4081559
openSNPrs4081559
23andMers4081559
23andMe allrs4081559
SNP Nexus

SNPshotrs4081559
SNPdbers4081559
MSV3drs4081559
GWAS Ctlgrs4081559
GMAF0.1088
Max Magnitude0
ClinVar
Risk rs4081559(A;A)
Alt rs4081559(A;A)
Reference rs4081559(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323677C>T
CLNSRC
CLNACC