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rs1050696

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1050696(C;C)
Make rs1050696(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356203
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050696
ebirs1050696
HLIrs1050696
Exacrs1050696
Varsomers1050696
Maprs1050696
PheGenIrs1050696
hapmaprs1050696
1000 genomesrs1050696
hgdprs1050696
ensemblrs1050696
gopubmedrs1050696
geneviewrs1050696
scholarrs1050696
googlers1050696
pharmgkbrs1050696
gwascentralrs1050696
openSNPrs1050696
23andMers1050696
23andMe allrs1050696
SNP Nexus

SNPshotrs1050696
SNPdbers1050696
MSV3drs1050696
GWAS Ctlgrs1050696
GMAF0.08907
Max Magnitude0
ClinVar
Risk rs1050696(C;C)
Alt rs1050696(C;C)
Reference rs1050696(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323980A>G
CLNSRC
CLNACC