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rs1050692

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050692(C;C)
Make rs1050692(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356214
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050692
ebirs1050692
HLIrs1050692
Exacrs1050692
Varsomers1050692
Maprs1050692
PheGenIrs1050692
hapmaprs1050692
1000 genomesrs1050692
hgdprs1050692
ensemblrs1050692
gopubmedrs1050692
geneviewrs1050692
scholarrs1050692
googlers1050692
pharmgkbrs1050692
gwascentralrs1050692
openSNPrs1050692
23andMers1050692
23andMe allrs1050692
SNP Nexus

SNPshotrs1050692
SNPdbers1050692
MSV3drs1050692
GWAS Ctlgrs1050692
GMAF0.0877
Max Magnitude0
ClinVar
Risk rs1050692(C,T;C,T)
Alt rs1050692(C,T;C,T)
Reference rs1050692(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323991C>A; NC_000006.11:g.31323991C>G
CLNSRC
CLNACC