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

rs9264601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264601(C;C)
Make rs9264601(C;T)
Make rs9264601(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269577
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264601
ebirs9264601
HLIrs9264601
Exacrs9264601
Varsomers9264601
Maprs9264601
PheGenIrs9264601
hapmaprs9264601
1000 genomesrs9264601
hgdprs9264601
ensemblrs9264601
gopubmedrs9264601
geneviewrs9264601
scholarrs9264601
googlers9264601
pharmgkbrs9264601
gwascentralrs9264601
openSNPrs9264601
23andMers9264601
23andMe allrs9264601
SNP Nexus

SNPshotrs9264601
SNPdbers9264601
MSV3drs9264601
GWAS Ctlgrs9264601
GMAF0.02525
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs9264601(A,C,T;A,C,T)
Alt rs9264601(A,C,T;A,C,T)
Reference rs9264601(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237354G>A
CLNSRC
CLNACC