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rs9264639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264639(C;T)
Make rs9264639(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270545
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264639
ebirs9264639
HLIrs9264639
Exacrs9264639
Varsomers9264639
Maprs9264639
PheGenIrs9264639
hapmaprs9264639
1000 genomesrs9264639
hgdprs9264639
ensemblrs9264639
gopubmedrs9264639
geneviewrs9264639
scholarrs9264639
googlers9264639
pharmgkbrs9264639
gwascentralrs9264639
openSNPrs9264639
23andMers9264639
23andMe allrs9264639
SNP Nexus

SNPshotrs9264639
SNPdbers9264639
MSV3drs9264639
GWAS Ctlgrs9264639
GMAF0.1093
Max Magnitude0
ClinVar
Risk rs9264639(T;T)
Alt rs9264639(T;T)
Reference rs9264639(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238322C>T
CLNSRC
CLNACC