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rs1131122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1131122(A;A)
Make rs1131122(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271599
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1131122
ebirs1131122
HLIrs1131122
Exacrs1131122
Varsomers1131122
Maprs1131122
PheGenIrs1131122
hapmaprs1131122
1000 genomesrs1131122
hgdprs1131122
ensemblrs1131122
gopubmedrs1131122
geneviewrs1131122
scholarrs1131122
googlers1131122
pharmgkbrs1131122
gwascentralrs1131122
openSNPrs1131122
23andMers1131122
23andMe allrs1131122
SNP Nexus

SNPshotrs1131122
SNPdbers1131122
MSV3drs1131122
GWAS Ctlgrs1131122
GMAF0.04086
Max Magnitude0
ClinVar
Risk rs1131122(A,C;A,C)
Alt rs1131122(A,C;A,C)
Reference rs1131122(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239376C>G; NC_000006.11:g.31239376C>T
CLNSRC
CLNACC