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rs9264666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264666(C;C)
Make rs9264666(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271519
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264666
ebirs9264666
HLIrs9264666
Exacrs9264666
Varsomers9264666
Maprs9264666
PheGenIrs9264666
hapmaprs9264666
1000 genomesrs9264666
hgdprs9264666
ensemblrs9264666
gopubmedrs9264666
geneviewrs9264666
scholarrs9264666
googlers9264666
pharmgkbrs9264666
gwascentralrs9264666
openSNPrs9264666
23andMers9264666
23andMe allrs9264666
SNP Nexus

SNPshotrs9264666
SNPdbers9264666
MSV3drs9264666
GWAS Ctlgrs9264666
GMAF0.4233
Max Magnitude0
ClinVar
Risk rs9264666(C;C)
Alt rs9264666(C;C)
Reference rs9264666(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239296G>C
CLNSRC
CLNACC