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rs1050379

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050379(C;T)
Make rs1050379(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356377
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050379
ebirs1050379
HLIrs1050379
Exacrs1050379
Varsomers1050379
Maprs1050379
PheGenIrs1050379
hapmaprs1050379
1000 genomesrs1050379
hgdprs1050379
ensemblrs1050379
gopubmedrs1050379
geneviewrs1050379
scholarrs1050379
googlers1050379
pharmgkbrs1050379
gwascentralrs1050379
openSNPrs1050379
23andMers1050379
23andMe allrs1050379
SNP Nexus

SNPshotrs1050379
SNPdbers1050379
MSV3drs1050379
GWAS Ctlgrs1050379
GMAF0.27
Max Magnitude0
ClinVar
Risk rs1050379(T;T)
Alt rs1050379(T;T)
Reference rs1050379(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324154G>A
CLNSRC
CLNACC