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rs1049709

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1049709(A;G)
Make rs1049709(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269077
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1049709
ebirs1049709
HLIrs1049709
Exacrs1049709
Varsomers1049709
Maprs1049709
PheGenIrs1049709
hapmaprs1049709
1000 genomesrs1049709
hgdprs1049709
ensemblrs1049709
gopubmedrs1049709
geneviewrs1049709
scholarrs1049709
googlers1049709
pharmgkbrs1049709
gwascentralrs1049709
openSNPrs1049709
23andMers1049709
23andMe allrs1049709
SNP Nexus

SNPshotrs1049709
SNPdbers1049709
MSV3drs1049709
GWAS Ctlgrs1049709
GMAF0.0652
Max Magnitude0
ClinVar
Risk rs1049709(G;G)
Alt rs1049709(G;G)
Reference rs1049709(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236854T; NC_000006.11:g.31236854T>C
CLNSRC
CLNACC