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rs76546355(A;A)

From SNPedia
increased risk of Behçet's disease
Is agenotype
ofrs76546355
Gene
Chromosome6
Position31,381,371
Merged fromRs116799036
mentionedby
Magnitude5.46
ReputeBad
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

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