Have questions? Visit https://www.reddit.com/r/SNPedia

rs9264628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264628(C;T)
Make rs9264628(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270194
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264628
ebirs9264628
HLIrs9264628
Exacrs9264628
Varsomers9264628
Maprs9264628
PheGenIrs9264628
hapmaprs9264628
1000 genomesrs9264628
hgdprs9264628
ensemblrs9264628
gopubmedrs9264628
geneviewrs9264628
scholarrs9264628
googlers9264628
pharmgkbrs9264628
gwascentralrs9264628
openSNPrs9264628
23andMers9264628
23andMe allrs9264628
SNP Nexus

SNPshotrs9264628
SNPdbers9264628
MSV3drs9264628
GWAS Ctlgrs9264628
GMAF0.3976
Max Magnitude0
ClinVar
Risk rs9264628(T;T)
Alt rs9264628(T;T)
Reference rs9264628(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237971C>T
CLNSRC
CLNACC