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rs1143551

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1143551(A;A)
Make rs1143551(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269983
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1143551
ebirs1143551
HLIrs1143551
Exacrs1143551
Varsomers1143551
Maprs1143551
PheGenIrs1143551
hapmaprs1143551
1000 genomesrs1143551
hgdprs1143551
ensemblrs1143551
gopubmedrs1143551
geneviewrs1143551
scholarrs1143551
googlers1143551
pharmgkbrs1143551
gwascentralrs1143551
openSNPrs1143551
23andMers1143551
23andMe allrs1143551
SNP Nexus

SNPshotrs1143551
SNPdbers1143551
MSV3drs1143551
GWAS Ctlgrs1143551
GMAF0.01882
Max Magnitude0
ClinVar
Risk rs1143551(A;A)
Alt rs1143551(A;A)
Reference rs1143551(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237760C>T
CLNSRC
CLNACC