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rs3176007

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3176007(C;C)
Make rs3176007(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269068
GeneHLA-C
is asnp
is mentioned by
dbSNPrs3176007
ebirs3176007
HLIrs3176007
Exacrs3176007
Varsomers3176007
Maprs3176007
PheGenIrs3176007
hapmaprs3176007
1000 genomesrs3176007
hgdprs3176007
ensemblrs3176007
gopubmedrs3176007
geneviewrs3176007
scholarrs3176007
googlers3176007
pharmgkbrs3176007
gwascentralrs3176007
openSNPrs3176007
23andMers3176007
23andMe allrs3176007
SNP Nexus

SNPshotrs3176007
SNPdbers3176007
MSV3drs3176007
GWAS Ctlgrs3176007
GMAF0.04913
Max Magnitude0
ClinVar
Risk rs3176007(C;C)
Alt rs3176007(C;C)
Reference rs3176007(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236845A>G
CLNSRC
CLNACC