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

rs9264626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264626(C;C)
Make rs9264626(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270185
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264626
ebirs9264626
HLIrs9264626
Exacrs9264626
Varsomers9264626
Maprs9264626
PheGenIrs9264626
hapmaprs9264626
1000 genomesrs9264626
hgdprs9264626
ensemblrs9264626
gopubmedrs9264626
geneviewrs9264626
scholarrs9264626
googlers9264626
pharmgkbrs9264626
gwascentralrs9264626
openSNPrs9264626
23andMers9264626
23andMe allrs9264626
SNP Nexus

SNPshotrs9264626
SNPdbers9264626
MSV3drs9264626
GWAS Ctlgrs9264626
GMAF0.3861
Max Magnitude0
ClinVar
Risk rs9264626(C;C)
Alt rs9264626(C;C)
Reference rs9264626(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237962T>C
CLNSRC
CLNACC