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rs9264637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264637(C;C)
Make rs9264637(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270531
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264637
ebirs9264637
HLIrs9264637
Exacrs9264637
Varsomers9264637
Maprs9264637
PheGenIrs9264637
hapmaprs9264637
1000 genomesrs9264637
hgdprs9264637
ensemblrs9264637
gopubmedrs9264637
geneviewrs9264637
scholarrs9264637
googlers9264637
pharmgkbrs9264637
gwascentralrs9264637
openSNPrs9264637
23andMers9264637
23andMe allrs9264637
SNP Nexus

SNPshotrs9264637
SNPdbers9264637
MSV3drs9264637
GWAS Ctlgrs9264637
GMAF0.2259
Max Magnitude0
ClinVar
Risk rs9264637(C;C)
Alt rs9264637(C;C)
Reference rs9264637(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238308G>C
CLNSRC
CLNACC