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rs1050459

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050459(A;A)
Make rs1050459(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357144
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050459
ebirs1050459
HLIrs1050459
Exacrs1050459
Varsomers1050459
Maprs1050459
PheGenIrs1050459
hapmaprs1050459
1000 genomesrs1050459
hgdprs1050459
ensemblrs1050459
gopubmedrs1050459
geneviewrs1050459
scholarrs1050459
googlers1050459
pharmgkbrs1050459
gwascentralrs1050459
openSNPrs1050459
23andMers1050459
23andMe allrs1050459
SNP Nexus

SNPshotrs1050459
SNPdbers1050459
MSV3drs1050459
GWAS Ctlgrs1050459
GMAF0.1616
Max Magnitude0
ClinVar
Risk rs1050459(A;A)
Alt rs1050459(A;A)
Reference rs1050459(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324921C>T
CLNSRC
CLNACC