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rs9264651

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264651(C;C)
Make rs9264651(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270951
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264651
ebirs9264651
HLIrs9264651
Exacrs9264651
Varsomers9264651
Maprs9264651
PheGenIrs9264651
hapmaprs9264651
1000 genomesrs9264651
hgdprs9264651
ensemblrs9264651
gopubmedrs9264651
geneviewrs9264651
scholarrs9264651
googlers9264651
pharmgkbrs9264651
gwascentralrs9264651
openSNPrs9264651
23andMers9264651
23andMe allrs9264651
SNP Nexus

SNPshotrs9264651
SNPdbers9264651
MSV3drs9264651
GWAS Ctlgrs9264651
Max Magnitude0
ClinVar
Risk rs9264651(C;C)
Alt rs9264651(C;C)
Reference rs9264651(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238728G>C
CLNSRC
CLNACC