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rs1049668

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1049668(A;A)
Make rs1049668(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269044
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1049668
ebirs1049668
HLIrs1049668
Exacrs1049668
Varsomers1049668
Maprs1049668
PheGenIrs1049668
hapmaprs1049668
1000 genomesrs1049668
hgdprs1049668
ensemblrs1049668
gopubmedrs1049668
geneviewrs1049668
scholarrs1049668
googlers1049668
pharmgkbrs1049668
gwascentralrs1049668
openSNPrs1049668
23andMers1049668
23andMe allrs1049668
SNP Nexus

SNPshotrs1049668
SNPdbers1049668
MSV3drs1049668
GWAS Ctlgrs1049668
GMAF0.02571
Max Magnitude0
ClinVar
Risk rs1049668(A;A)
Alt rs1049668(A;A)
Reference rs1049668(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236821C>T
CLNSRC
CLNACC