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rs9264623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264623(C;C)
Make rs9264623(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270173
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264623
ebirs9264623
HLIrs9264623
Exacrs9264623
Varsomers9264623
Maprs9264623
PheGenIrs9264623
hapmaprs9264623
1000 genomesrs9264623
hgdprs9264623
ensemblrs9264623
gopubmedrs9264623
geneviewrs9264623
scholarrs9264623
googlers9264623
pharmgkbrs9264623
gwascentralrs9264623
openSNPrs9264623
23andMers9264623
23andMe allrs9264623
SNP Nexus

SNPshotrs9264623
SNPdbers9264623
MSV3drs9264623
GWAS Ctlgrs9264623
GMAF0.3118
Max Magnitude0
ClinVar
Risk rs9264623(C;C)
Alt rs9264623(C;C)
Reference rs9264623(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237950T>C
CLNSRC
CLNACC