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rs9264629

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264629(C;C)
Make rs9264629(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270198
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264629
ebirs9264629
HLIrs9264629
Exacrs9264629
Varsomers9264629
Maprs9264629
PheGenIrs9264629
hapmaprs9264629
1000 genomesrs9264629
hgdprs9264629
ensemblrs9264629
gopubmedrs9264629
geneviewrs9264629
scholarrs9264629
googlers9264629
pharmgkbrs9264629
gwascentralrs9264629
openSNPrs9264629
23andMers9264629
23andMe allrs9264629
SNP Nexus

SNPshotrs9264629
SNPdbers9264629
MSV3drs9264629
GWAS Ctlgrs9264629
GMAF0.3939
Max Magnitude0
ClinVar
Risk rs9264629(C;C)
Alt rs9264629(C;C)
Reference rs9264629(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237975T>C
CLNSRC
CLNACC