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rs28367581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28367581(C;C)
Make rs28367581(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271469
GeneHLA-C
is asnp
is mentioned by
dbSNPrs28367581
ebirs28367581
HLIrs28367581
Exacrs28367581
Varsomers28367581
Maprs28367581
PheGenIrs28367581
hapmaprs28367581
1000 genomesrs28367581
hgdprs28367581
ensemblrs28367581
gopubmedrs28367581
geneviewrs28367581
scholarrs28367581
googlers28367581
pharmgkbrs28367581
gwascentralrs28367581
openSNPrs28367581
23andMers28367581
23andMe allrs28367581
SNP Nexus

SNPshotrs28367581
SNPdbers28367581
MSV3drs28367581
GWAS Ctlgrs28367581
GMAF0.04867
Max Magnitude0
ClinVar
Risk rs28367581(C;C)
Alt rs28367581(C;C)
Reference rs28367581(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239246T>C
CLNSRC
CLNACC