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rs9461679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9461679(A;A)
Make rs9461679(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270094
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9461679
ebirs9461679
HLIrs9461679
Exacrs9461679
Varsomers9461679
Maprs9461679
PheGenIrs9461679
hapmaprs9461679
1000 genomesrs9461679
hgdprs9461679
ensemblrs9461679
gopubmedrs9461679
geneviewrs9461679
scholarrs9461679
googlers9461679
pharmgkbrs9461679
gwascentralrs9461679
openSNPrs9461679
23andMers9461679
23andMe allrs9461679
SNP Nexus

SNPshotrs9461679
SNPdbers9461679
MSV3drs9461679
GWAS Ctlgrs9461679
GMAF0.01699
Max Magnitude0
ClinVar
Risk rs9461679(A;A)
Alt rs9461679(A;A)
Reference rs9461679(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237871G>A
CLNSRC
CLNACC