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rs9264661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264661(C;T)
Make rs9264661(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271364
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264661
ebirs9264661
HLIrs9264661
Exacrs9264661
Varsomers9264661
Maprs9264661
PheGenIrs9264661
hapmaprs9264661
1000 genomesrs9264661
hgdprs9264661
ensemblrs9264661
gopubmedrs9264661
geneviewrs9264661
scholarrs9264661
googlers9264661
pharmgkbrs9264661
gwascentralrs9264661
openSNPrs9264661
23andMers9264661
23andMe allrs9264661
SNP Nexus

SNPshotrs9264661
SNPdbers9264661
MSV3drs9264661
GWAS Ctlgrs9264661
GMAF0.4215
Max Magnitude0
ClinVar
Risk rs9264661(T;T)
Alt rs9264661(T;T)
Reference rs9264661(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239141C>T
CLNSRC
CLNACC