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rs1050747

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs1050747(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355519
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050747
ebirs1050747
HLIrs1050747
Exacrs1050747
Varsomers1050747
Maprs1050747
PheGenIrs1050747
hapmaprs1050747
1000 genomesrs1050747
hgdprs1050747
ensemblrs1050747
gopubmedrs1050747
geneviewrs1050747
scholarrs1050747
googlers1050747
pharmgkbrs1050747
gwascentralrs1050747
openSNPrs1050747
23andMers1050747
23andMe allrs1050747
SNP Nexus

SNPshotrs1050747
SNPdbers1050747
MSV3drs1050747
GWAS Ctlgrs1050747
GMAF0.1781
Max Magnitude0
ClinVar
Risk rs1050747(C;C)
Alt rs1050747(C;C)
Reference rs1050747(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323296A>G
CLNSRC
CLNACC