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rs9264644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264644(C;T)
Make rs9264644(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270745
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264644
ebirs9264644
HLIrs9264644
Exacrs9264644
Varsomers9264644
Maprs9264644
PheGenIrs9264644
hapmaprs9264644
1000 genomesrs9264644
hgdprs9264644
ensemblrs9264644
gopubmedrs9264644
geneviewrs9264644
scholarrs9264644
googlers9264644
pharmgkbrs9264644
gwascentralrs9264644
openSNPrs9264644
23andMers9264644
23andMe allrs9264644
SNP Nexus

SNPshotrs9264644
SNPdbers9264644
MSV3drs9264644
GWAS Ctlgrs9264644
GMAF0.2355
Max Magnitude0
ClinVar
Risk rs9264644(T;T)
Alt rs9264644(T;T)
Reference rs9264644(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238522C>T
CLNSRC
CLNACC