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rs1050564

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050564(A;A)
Make rs1050564(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356785
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050564
ebirs1050564
HLIrs1050564
Exacrs1050564
Varsomers1050564
Maprs1050564
PheGenIrs1050564
hapmaprs1050564
1000 genomesrs1050564
hgdprs1050564
ensemblrs1050564
gopubmedrs1050564
geneviewrs1050564
scholarrs1050564
googlers1050564
pharmgkbrs1050564
gwascentralrs1050564
openSNPrs1050564
23andMers1050564
23andMe allrs1050564
SNP Nexus

SNPshotrs1050564
SNPdbers1050564
MSV3drs1050564
GWAS Ctlgrs1050564
GMAF0.07484
Max Magnitude0
ClinVar
Risk rs1050564(A,T;A,T)
Alt rs1050564(A,T;A,T)
Reference rs1050564(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324562C>A; NC_000006.11:g.31324562C>T
CLNSRC
CLNACC