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rs9264641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264641(C;C)
Make rs9264641(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270600
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264641
ebirs9264641
HLIrs9264641
Exacrs9264641
Varsomers9264641
Maprs9264641
PheGenIrs9264641
hapmaprs9264641
1000 genomesrs9264641
hgdprs9264641
ensemblrs9264641
gopubmedrs9264641
geneviewrs9264641
scholarrs9264641
googlers9264641
pharmgkbrs9264641
gwascentralrs9264641
openSNPrs9264641
23andMers9264641
23andMe allrs9264641
SNP Nexus

SNPshotrs9264641
SNPdbers9264641
MSV3drs9264641
GWAS Ctlgrs9264641
GMAF0.06107
Max Magnitude0
ClinVar
Risk rs9264641(C;C)
Alt rs9264641(C;C)
Reference rs9264641(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238377G; NC_000006.11:g.31238377G>C
CLNSRC
CLNACC