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rs13214791

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs13214791(G;T)
Make rs13214791(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354985
GeneHLA-B
is asnp
is mentioned by
dbSNPrs13214791
ebirs13214791
HLIrs13214791
Exacrs13214791
Varsomers13214791
Maprs13214791
PheGenIrs13214791
hapmaprs13214791
1000 genomesrs13214791
hgdprs13214791
ensemblrs13214791
gopubmedrs13214791
geneviewrs13214791
scholarrs13214791
googlers13214791
pharmgkbrs13214791
gwascentralrs13214791
openSNPrs13214791
23andMers13214791
23andMe allrs13214791
SNP Nexus

SNPshotrs13214791
SNPdbers13214791
MSV3drs13214791
GWAS Ctlgrs13214791
GMAF0.03444
Max Magnitude0
ClinVar
Risk rs13214791(T;T)
Alt rs13214791(T;T)
Reference rs13214791(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322762G>T
CLNSRC
CLNACC