increased risk of Behçet's disease |
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 25889189] Characterization of the major histocompatibility complex locus association with Behçet's disease in Iran