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rs76546355

From SNPedia

(A) allele has increased risk of Behçet's disease
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 5.46 increased risk of Behçet's disease
(A;G) 5.46 increased risk of Behçet's disease
(G;G) 0 common in complete genomics
ReferenceGRCh38 38.1/141
Chromosome6
Position31381371
is asnp
is mentioned by
dbSNPrs76546355
ebirs76546355
HLIrs76546355
Exacrs76546355
Varsomers76546355
Maprs76546355
PheGenIrs76546355
hapmaprs76546355
1000 genomesrs76546355
hgdprs76546355
ensemblrs76546355
gopubmedrs76546355
geneviewrs76546355
scholarrs76546355
googlers76546355
pharmgkbrs76546355
gwascentralrs76546355
openSNPrs76546355
23andMers76546355
23andMe allrs76546355
SNP Nexus

SNPshotrs76546355
SNPdbers76546355
MSV3drs76546355
GWAS Ctlgrs76546355
Merged fromRs116799036
Max Magnitude5.46

rs76546355 (A) is a risk allele for Behçet's disease.

HLA-B*51 allele and the rs76546355 MHC SNP are independent genetic risk factors for Behçet's disease in Iranian, and that positivity for the rs76546355 risk allele, but not for B*51, does correlate with specific demographic characteristics or clinical manifestations in Behçet's disease patients

[PMID 25889189OA-icon.png] Characterization of the major histocompatibility complex locus association with Behçet's disease in Iran