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rs9264607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264607(A;A)
Make rs9264607(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269828
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264607
ebirs9264607
HLIrs9264607
Exacrs9264607
Varsomers9264607
Maprs9264607
PheGenIrs9264607
hapmaprs9264607
1000 genomesrs9264607
hgdprs9264607
ensemblrs9264607
gopubmedrs9264607
geneviewrs9264607
scholarrs9264607
googlers9264607
pharmgkbrs9264607
gwascentralrs9264607
openSNPrs9264607
23andMers9264607
23andMe allrs9264607
SNP Nexus

SNPshotrs9264607
SNPdbers9264607
MSV3drs9264607
GWAS Ctlgrs9264607
GMAF0.2296
Max Magnitude0
ClinVar
Risk rs9264607(A;A)
Alt rs9264607(A;A)
Reference rs9264607(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237605G>A
CLNSRC
CLNACC