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rs9264609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264609(C;T)
Make rs9264609(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269887
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264609
ebirs9264609
HLIrs9264609
Exacrs9264609
Varsomers9264609
Maprs9264609
PheGenIrs9264609
hapmaprs9264609
1000 genomesrs9264609
hgdprs9264609
ensemblrs9264609
gopubmedrs9264609
geneviewrs9264609
scholarrs9264609
googlers9264609
pharmgkbrs9264609
gwascentralrs9264609
openSNPrs9264609
23andMers9264609
23andMe allrs9264609
SNP Nexus

SNPshotrs9264609
SNPdbers9264609
MSV3drs9264609
GWAS Ctlgrs9264609
GMAF0.2208
Max Magnitude0
ClinVar
Risk rs9264609(T;T)
Alt rs9264609(T;T)
Reference rs9264609(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237664C>T
CLNSRC
CLNACC