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rs9264653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264653(C;C)
Make rs9264653(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271037
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264653
ebirs9264653
HLIrs9264653
Exacrs9264653
Varsomers9264653
Maprs9264653
PheGenIrs9264653
hapmaprs9264653
1000 genomesrs9264653
hgdprs9264653
ensemblrs9264653
gopubmedrs9264653
geneviewrs9264653
scholarrs9264653
googlers9264653
pharmgkbrs9264653
gwascentralrs9264653
openSNPrs9264653
23andMers9264653
23andMe allrs9264653
SNP Nexus

SNPshotrs9264653
SNPdbers9264653
MSV3drs9264653
GWAS Ctlgrs9264653
GMAF0.3848
Max Magnitude0
ClinVar
Risk rs9264653(C;C)
Alt rs9264653(C;C)
Reference rs9264653(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238814T>C
CLNSRC
CLNACC