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rs9264625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264625(C;C)
Make rs9264625(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270183
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264625
ebirs9264625
HLIrs9264625
Exacrs9264625
Varsomers9264625
Maprs9264625
PheGenIrs9264625
hapmaprs9264625
1000 genomesrs9264625
hgdprs9264625
ensemblrs9264625
gopubmedrs9264625
geneviewrs9264625
scholarrs9264625
googlers9264625
pharmgkbrs9264625
gwascentralrs9264625
openSNPrs9264625
23andMers9264625
23andMe allrs9264625
SNP Nexus

SNPshotrs9264625
SNPdbers9264625
MSV3drs9264625
GWAS Ctlgrs9264625
GMAF0.3586
Max Magnitude0
ClinVar
Risk rs9264625(C;C)
Alt rs9264625(C;C)
Reference rs9264625(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237960G>C
CLNSRC
CLNACC