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rs9264652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264652(C;C)
Make rs9264652(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270985
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264652
ebirs9264652
HLIrs9264652
Exacrs9264652
Varsomers9264652
Maprs9264652
PheGenIrs9264652
hapmaprs9264652
1000 genomesrs9264652
hgdprs9264652
ensemblrs9264652
gopubmedrs9264652
geneviewrs9264652
scholarrs9264652
googlers9264652
pharmgkbrs9264652
gwascentralrs9264652
openSNPrs9264652
23andMers9264652
23andMe allrs9264652
SNP Nexus

SNPshotrs9264652
SNPdbers9264652
MSV3drs9264652
GWAS Ctlgrs9264652
GMAF0.2195
Max Magnitude0
ClinVar
Risk rs9264652(C;C)
Alt rs9264652(C;C)
Reference rs9264652(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238762T>C
CLNSRC
CLNACC