Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10515746
rs10515746
Entrez Id: 84868
Gene Symbol: HAVCR2
HAVCR2
CUI: C0004943
Disease:
Behcet Syndrome 		0.010 GeneticVariation BEFREE Two single-nucleotide polymorphisms of TIM-3 (rs9313439 and rs10515746) were genotyped in 212 patients with Behçet disease and 200 healthy controls. 31644615 2019