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rs1050462

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050462(C;C)
Make rs1050462(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357134
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050462
ebirs1050462
HLIrs1050462
Exacrs1050462
Varsomers1050462
Maprs1050462
PheGenIrs1050462
hapmaprs1050462
1000 genomesrs1050462
hgdprs1050462
ensemblrs1050462
gopubmedrs1050462
geneviewrs1050462
scholarrs1050462
googlers1050462
pharmgkbrs1050462
gwascentralrs1050462
openSNPrs1050462
23andMers1050462
23andMe allrs1050462
SNP Nexus

SNPshotrs1050462
SNPdbers1050462
MSV3drs1050462
GWAS Ctlgrs1050462
GMAF0.2268
Max Magnitude0
ClinVar
Risk rs1050462(C;C)
Alt rs1050462(C;C)
Reference rs1050462(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324911C>G
CLNSRC
CLNACC