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rs9264636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264636(C;T)
Make rs9264636(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270520
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264636
ebirs9264636
HLIrs9264636
Exacrs9264636
Varsomers9264636
Maprs9264636
PheGenIrs9264636
hapmaprs9264636
1000 genomesrs9264636
hgdprs9264636
ensemblrs9264636
gopubmedrs9264636
geneviewrs9264636
scholarrs9264636
googlers9264636
pharmgkbrs9264636
gwascentralrs9264636
openSNPrs9264636
23andMers9264636
23andMe allrs9264636
SNP Nexus

SNPshotrs9264636
SNPdbers9264636
MSV3drs9264636
GWAS Ctlgrs9264636
GMAF0.225
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs9264636(T;T)
Alt rs9264636(T;T)
Reference rs9264636(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238297C>T
CLNSRC
CLNACC