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rs9264646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264646(C;C)
Make rs9264646(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270758
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264646
ebirs9264646
HLIrs9264646
Exacrs9264646
Varsomers9264646
Maprs9264646
PheGenIrs9264646
hapmaprs9264646
1000 genomesrs9264646
hgdprs9264646
ensemblrs9264646
gopubmedrs9264646
geneviewrs9264646
scholarrs9264646
googlers9264646
pharmgkbrs9264646
gwascentralrs9264646
openSNPrs9264646
23andMers9264646
23andMe allrs9264646
SNP Nexus

SNPshotrs9264646
SNPdbers9264646
MSV3drs9264646
GWAS Ctlgrs9264646
GMAF0.2479
Max Magnitude0
ClinVar
Risk rs9264646(C;C)
Alt rs9264646(C;C)
Reference rs9264646(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238535T>C
CLNSRC
CLNACC