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rs1050393

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1050393(A;G)
Make rs1050393(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356742
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050393
ebirs1050393
HLIrs1050393
Exacrs1050393
Varsomers1050393
Maprs1050393
PheGenIrs1050393
hapmaprs1050393
1000 genomesrs1050393
hgdprs1050393
ensemblrs1050393
gopubmedrs1050393
geneviewrs1050393
scholarrs1050393
googlers1050393
pharmgkbrs1050393
gwascentralrs1050393
openSNPrs1050393
23andMers1050393
23andMe allrs1050393
SNP Nexus

SNPshotrs1050393
SNPdbers1050393
MSV3drs1050393
GWAS Ctlgrs1050393
Max Magnitude0
ClinVar
Risk rs1050393(G;G)
Alt rs1050393(G;G)
Reference rs1050393(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324519T>C
CLNSRC
CLNACC