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rs16899066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs16899066(C;C)
Make rs16899066(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355803
GeneHLA-B
is asnp
is mentioned by
dbSNPrs16899066
ebirs16899066
HLIrs16899066
Exacrs16899066
Varsomers16899066
Maprs16899066
PheGenIrs16899066
hapmaprs16899066
1000 genomesrs16899066
hgdprs16899066
ensemblrs16899066
gopubmedrs16899066
geneviewrs16899066
scholarrs16899066
googlers16899066
pharmgkbrs16899066
gwascentralrs16899066
openSNPrs16899066
23andMers16899066
23andMe allrs16899066
SNP Nexus

SNPshotrs16899066
SNPdbers16899066
MSV3drs16899066
GWAS Ctlgrs16899066
GMAF0.01699
Max Magnitude0
ClinVar
Risk rs16899066(C;C)
Alt rs16899066(C;C)
Reference rs16899066(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323580T>C
CLNSRC
CLNACC