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rs9264663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264663(C;T)
Make rs9264663(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271428
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264663
ebirs9264663
HLIrs9264663
Exacrs9264663
Varsomers9264663
Maprs9264663
PheGenIrs9264663
hapmaprs9264663
1000 genomesrs9264663
hgdprs9264663
ensemblrs9264663
gopubmedrs9264663
geneviewrs9264663
scholarrs9264663
googlers9264663
pharmgkbrs9264663
gwascentralrs9264663
openSNPrs9264663
23andMers9264663
23andMe allrs9264663
SNP Nexus

SNPshotrs9264663
SNPdbers9264663
MSV3drs9264663
GWAS Ctlgrs9264663
GMAF0.2319
Max Magnitude0
ClinVar
Risk rs9264663(T;T)
Alt rs9264663(T;T)
Reference rs9264663(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239205C>T
CLNSRC
CLNACC