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rs9264642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9264642(C;C)
Make rs9264642(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270713
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264642
ebirs9264642
HLIrs9264642
Exacrs9264642
Varsomers9264642
Maprs9264642
PheGenIrs9264642
hapmaprs9264642
1000 genomesrs9264642
hgdprs9264642
ensemblrs9264642
gopubmedrs9264642
geneviewrs9264642
scholarrs9264642
googlers9264642
pharmgkbrs9264642
gwascentralrs9264642
openSNPrs9264642
23andMers9264642
23andMe allrs9264642
SNP Nexus

SNPshotrs9264642
SNPdbers9264642
MSV3drs9264642
GWAS Ctlgrs9264642
GMAF0.2704
Max Magnitude0
ClinVar
Risk rs9264642(C;C)
Alt rs9264642(C;C)
Reference rs9264642(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238490T>C
CLNSRC
CLNACC