Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7574070
rs7574070
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		A 0.810 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs7574070
rs7574070
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012