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rs9264627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264627(A;A)
Make rs9264627(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270186
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264627
ebirs9264627
HLIrs9264627
Exacrs9264627
Varsomers9264627
Maprs9264627
PheGenIrs9264627
hapmaprs9264627
1000 genomesrs9264627
hgdprs9264627
ensemblrs9264627
gopubmedrs9264627
geneviewrs9264627
scholarrs9264627
googlers9264627
pharmgkbrs9264627
gwascentralrs9264627
openSNPrs9264627
23andMers9264627
23andMe allrs9264627
SNP Nexus

SNPshotrs9264627
SNPdbers9264627
MSV3drs9264627
GWAS Ctlgrs9264627
GMAF0.3852
Max Magnitude0
ClinVar
Risk rs9264627(A;A)
Alt rs9264627(A;A)
Reference rs9264627(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237963G>A
CLNSRC
CLNACC