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rs4990036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs4990036(C;T)
Make rs4990036(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355729
GeneHLA-B
is asnp
is mentioned by
dbSNPrs4990036
ebirs4990036
HLIrs4990036
Exacrs4990036
Varsomers4990036
Maprs4990036
PheGenIrs4990036
hapmaprs4990036
1000 genomesrs4990036
hgdprs4990036
ensemblrs4990036
gopubmedrs4990036
geneviewrs4990036
scholarrs4990036
googlers4990036
pharmgkbrs4990036
gwascentralrs4990036
openSNPrs4990036
23andMers4990036
23andMe allrs4990036
SNP Nexus

SNPshotrs4990036
SNPdbers4990036
MSV3drs4990036
GWAS Ctlgrs4990036
GMAF0.07117
Max Magnitude0
ClinVar
Risk rs4990036(T;T)
Alt rs4990036(T;T)
Reference rs4990036(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323506C>T
CLNSRC
CLNACC