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rs79556279

From SNPedia
(T) allele has increased risk of Behçet's disease
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
(G;T) 4.11 increased risk of Behçet's disease
(T;T) 4.11 increased risk of Behçet's disease
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position31362069
is asnp
is mentioned by
dbSNPrs79556279
dbSNP (old)rs79556279
ClinGenrs79556279
ebirs79556279
HLIrs79556279
Exacrs79556279
Gnomadrs79556279
Varsomers79556279
Maprs79556279
PheGenIrs79556279
Biobankrs79556279
1000 genomesrs79556279
hgdprs79556279
ensemblrs79556279
gopubmedrs79556279
geneviewrs79556279
scholarrs79556279
googlers79556279
pharmgkbrs79556279
gwascentralrs79556279
openSNPrs79556279
23andMers79556279
23andMe allrs79556279
SNP Nexus

SNPshotrs79556279
SNPdbers79556279
MSV3drs79556279
GWAS Ctlgrs79556279
Max Magnitude4.11

Primary risk for Behçet's disease associated with the minor (T) allele of rs79556279 [PMID 24821759OA-icon.png] [PMID 24876276OA-icon.png] [PMID 24286189OA-icon.png]


A meta-analysis totaling ~5,000 Behçet's disease (BD) patients from 78 independent studies calculated a pooled odds ratio of 5.78 (CI: 5.0-6.7) for HLA-B51/B5 allele carriers to develop BD compared with noncarriers.[PMID 19790126OA-icon.png]