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rs9264603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264603(C;C)
Make rs9264603(C;T)
Make rs9264603(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269661
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264603
ebirs9264603
HLIrs9264603
Exacrs9264603
Varsomers9264603
Maprs9264603
PheGenIrs9264603
hapmaprs9264603
1000 genomesrs9264603
hgdprs9264603
ensemblrs9264603
gopubmedrs9264603
geneviewrs9264603
scholarrs9264603
googlers9264603
pharmgkbrs9264603
gwascentralrs9264603
openSNPrs9264603
23andMers9264603
23andMe allrs9264603
SNP Nexus

SNPshotrs9264603
SNPdbers9264603
MSV3drs9264603
GWAS Ctlgrs9264603
GMAF0.04224
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs9264603(A,C,T;A,C,T)
Alt rs9264603(A,C,T;A,C,T)
Reference rs9264603(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237438G>A
CLNSRC
CLNACC