Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17006292
rs17006292
TFCP2L1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASCAT Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs17006292
rs17006292
TFCP2L1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012