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rs1131165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1131165(C;G)
Make rs1131165(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357110
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1131165
ebirs1131165
HLIrs1131165
Exacrs1131165
Varsomers1131165
Maprs1131165
PheGenIrs1131165
hapmaprs1131165
1000 genomesrs1131165
hgdprs1131165
ensemblrs1131165
gopubmedrs1131165
geneviewrs1131165
scholarrs1131165
googlers1131165
pharmgkbrs1131165
gwascentralrs1131165
openSNPrs1131165
23andMers1131165
23andMe allrs1131165
SNP Nexus

SNPshotrs1131165
SNPdbers1131165
MSV3drs1131165
GWAS Ctlgrs1131165
GMAF0.4362
Max Magnitude0
ClinVar
Risk rs1131165(G;G)
Alt rs1131165(G;G)
Reference rs1131165(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324887G>C
CLNSRC
CLNACC