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rs9264622

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9264622(A;G)
Make rs9264622(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270099
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264622
ebirs9264622
HLIrs9264622
Exacrs9264622
Varsomers9264622
Maprs9264622
PheGenIrs9264622
hapmaprs9264622
1000 genomesrs9264622
hgdprs9264622
ensemblrs9264622
gopubmedrs9264622
geneviewrs9264622
scholarrs9264622
googlers9264622
pharmgkbrs9264622
gwascentralrs9264622
openSNPrs9264622
23andMers9264622
23andMe allrs9264622
SNP Nexus

SNPshotrs9264622
SNPdbers9264622
MSV3drs9264622
GWAS Ctlgrs9264622
GMAF0.2323
Max Magnitude0
ClinVar
Risk rs9264622(G;G)
Alt rs9264622(G;G)
Reference rs9264622(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237876A>G
CLNSRC
CLNACC