Have questions? Visit https://www.reddit.com/r/SNPedia

rs28367580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28367580(C;G)
Make rs28367580(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271380
GeneHLA-C
is asnp
is mentioned by
dbSNPrs28367580
ebirs28367580
HLIrs28367580
Exacrs28367580
Varsomers28367580
Maprs28367580
PheGenIrs28367580
hapmaprs28367580
1000 genomesrs28367580
hgdprs28367580
ensemblrs28367580
gopubmedrs28367580
geneviewrs28367580
scholarrs28367580
googlers28367580
pharmgkbrs28367580
gwascentralrs28367580
openSNPrs28367580
23andMers28367580
23andMe allrs28367580
SNP Nexus

SNPshotrs28367580
SNPdbers28367580
MSV3drs28367580
GWAS Ctlgrs28367580
GMAF0.04316
Max Magnitude0
ClinVar
Risk rs28367580(G;G)
Alt rs28367580(G;G)
Reference rs28367580(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239157C>G
CLNSRC
CLNACC