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rs9264624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264624(G;G)
Make rs9264624(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270178
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264624
ebirs9264624
HLIrs9264624
Exacrs9264624
Varsomers9264624
Maprs9264624
PheGenIrs9264624
hapmaprs9264624
1000 genomesrs9264624
hgdprs9264624
ensemblrs9264624
gopubmedrs9264624
geneviewrs9264624
scholarrs9264624
googlers9264624
pharmgkbrs9264624
gwascentralrs9264624
openSNPrs9264624
23andMers9264624
23andMe allrs9264624
SNP Nexus

SNPshotrs9264624
SNPdbers9264624
MSV3drs9264624
GWAS Ctlgrs9264624
GMAF0.3287
Max Magnitude0
ClinVar
Risk rs9264624(G;G)
Alt rs9264624(G;G)
Reference rs9264624(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237955T>G
CLNSRC
CLNACC