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rs9264665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264665(C;C)
Make rs9264665(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271502
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264665
ebirs9264665
HLIrs9264665
Exacrs9264665
Varsomers9264665
Maprs9264665
PheGenIrs9264665
hapmaprs9264665
1000 genomesrs9264665
hgdprs9264665
ensemblrs9264665
gopubmedrs9264665
geneviewrs9264665
scholarrs9264665
googlers9264665
pharmgkbrs9264665
gwascentralrs9264665
openSNPrs9264665
23andMers9264665
23andMe allrs9264665
SNP Nexus

SNPshotrs9264665
SNPdbers9264665
MSV3drs9264665
GWAS Ctlgrs9264665
Max Magnitude0
ClinVar
Risk rs9264665(C;C)
Alt rs9264665(C;C)
Reference rs9264665(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239279T>C
CLNSRC
CLNACC