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rs1049663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1049663(G;T)
Make rs1049663(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269036
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1049663
ebirs1049663
HLIrs1049663
Exacrs1049663
Varsomers1049663
Maprs1049663
PheGenIrs1049663
hapmaprs1049663
1000 genomesrs1049663
hgdprs1049663
ensemblrs1049663
gopubmedrs1049663
geneviewrs1049663
scholarrs1049663
googlers1049663
pharmgkbrs1049663
gwascentralrs1049663
openSNPrs1049663
23andMers1049663
23andMe allrs1049663
SNP Nexus

SNPshotrs1049663
SNPdbers1049663
MSV3drs1049663
GWAS Ctlgrs1049663
GMAF0.02663
Max Magnitude0
ClinVar
Risk rs1049663(T;T)
Alt rs1049663(T;T)
Reference rs1049663(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236813C>A
CLNSRC
CLNACC