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rs76486921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs76486921(A;G)
Make rs76486921(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269951
GeneHLA-C
is asnp
is mentioned by
dbSNPrs76486921
ebirs76486921
HLIrs76486921
Exacrs76486921
Varsomers76486921
Maprs76486921
PheGenIrs76486921
hapmaprs76486921
1000 genomesrs76486921
hgdprs76486921
ensemblrs76486921
gopubmedrs76486921
geneviewrs76486921
scholarrs76486921
googlers76486921
pharmgkbrs76486921
gwascentralrs76486921
openSNPrs76486921
23andMers76486921
23andMe allrs76486921
SNP Nexus

SNPshotrs76486921
SNPdbers76486921
MSV3drs76486921
GWAS Ctlgrs76486921
Max Magnitude0
ClinVar
Risk rs76486921(G;G)
Alt rs76486921(G;G)
Reference rs76486921(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237728T>C
CLNSRC
CLNACC