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rs1050147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1050147(C;C)
Make rs1050147(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270025
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050147
ebirs1050147
HLIrs1050147
Exacrs1050147
Varsomers1050147
Maprs1050147
PheGenIrs1050147
hapmaprs1050147
1000 genomesrs1050147
hgdprs1050147
ensemblrs1050147
gopubmedrs1050147
geneviewrs1050147
scholarrs1050147
googlers1050147
pharmgkbrs1050147
gwascentralrs1050147
openSNPrs1050147
23andMers1050147
23andMe allrs1050147
SNP Nexus

SNPshotrs1050147
SNPdbers1050147
MSV3drs1050147
GWAS Ctlgrs1050147
GMAF0.2296
Max Magnitude0
ClinVar
Risk rs1050147(C;C)
Alt rs1050147(C;C)
Reference rs1050147(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237802A>G
CLNSRC
CLNACC