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rs1050538

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1050538(A;C)
Make rs1050538(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356822
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050538
ebirs1050538
HLIrs1050538
Exacrs1050538
Varsomers1050538
Maprs1050538
PheGenIrs1050538
hapmaprs1050538
1000 genomesrs1050538
hgdprs1050538
ensemblrs1050538
gopubmedrs1050538
geneviewrs1050538
scholarrs1050538
googlers1050538
pharmgkbrs1050538
gwascentralrs1050538
openSNPrs1050538
23andMers1050538
23andMe allrs1050538
SNP Nexus

SNPshotrs1050538
SNPdbers1050538
MSV3drs1050538
GWAS Ctlgrs1050538
Max Magnitude0
ClinVar
Risk rs1050538(C,G;C,G)
Alt rs1050538(C,G;C,G)
Reference rs1050538(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324599T>C; NC_000006.11:g.31324599T>G
CLNSRC
CLNACC