Have questions? Visit https://www.reddit.com/r/SNPedia

rs9264606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9264606(A;C)
Make rs9264606(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269815
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264606
ebirs9264606
HLIrs9264606
Exacrs9264606
Varsomers9264606
Maprs9264606
PheGenIrs9264606
hapmaprs9264606
1000 genomesrs9264606
hgdprs9264606
ensemblrs9264606
gopubmedrs9264606
geneviewrs9264606
scholarrs9264606
googlers9264606
pharmgkbrs9264606
gwascentralrs9264606
openSNPrs9264606
23andMers9264606
23andMe allrs9264606
SNP Nexus

SNPshotrs9264606
SNPdbers9264606
MSV3drs9264606
GWAS Ctlgrs9264606
GMAF0.2231
Max Magnitude0
? (A;A) (A;C) (C;C) 28
ClinVar
Risk rs9264606(C;C)
Alt rs9264606(C;C)
Reference rs9264606(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237592A>C
CLNSRC
CLNACC