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rs9264640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9264640(C;G)
Make rs9264640(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270595
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264640
dbSNP (classic)rs9264640
ClinGenrs9264640
ebirs9264640
HLIrs9264640
Exacrs9264640
Gnomadrs9264640
Varsomers9264640
LitVarrs9264640
Maprs9264640
PheGenIrs9264640
Biobankrs9264640
1000 genomesrs9264640
hgdprs9264640
ensemblrs9264640
geneviewrs9264640
scholarrs9264640
googlers9264640
pharmgkbrs9264640
gwascentralrs9264640
openSNPrs9264640
23andMers9264640
SNPshotrs9264640
SNPdbers9264640
MSV3drs9264640
GWAS Ctlgrs9264640
GMAF0.2213
Max Magnitude0
ClinVar
Risk rs9264640(G;G)
Alt rs9264640(G;G)
Reference Rs9264640(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238372C>G
CLNSRC
CLNACC