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rs9264664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264664(C;T)
Make rs9264664(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271450
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264664
ebirs9264664
HLIrs9264664
Exacrs9264664
Varsomers9264664
Maprs9264664
PheGenIrs9264664
hapmaprs9264664
1000 genomesrs9264664
hgdprs9264664
ensemblrs9264664
gopubmedrs9264664
geneviewrs9264664
scholarrs9264664
googlers9264664
pharmgkbrs9264664
gwascentralrs9264664
openSNPrs9264664
23andMers9264664
23andMe allrs9264664
SNP Nexus

SNPshotrs9264664
SNPdbers9264664
MSV3drs9264664
GWAS Ctlgrs9264664
GMAF0.2585
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs9264664(T;T)
Alt rs9264664(T;T)
Reference rs9264664(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239227C>T
CLNSRC
CLNACC