ITGAL, integrin subunit alpha L, 3683

N. diseases: 169; N. variants: 8
Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11574944
rs11574944
Entrez Id: 3683
Gene Symbol: ITGAL
ITGAL
CUI: C0004943
Disease:
Behcet Syndrome 		0.010 GeneticVariation BEFREE The frequencies of genotype rs11574944 CC and haplotype rs11574944C-rs2230433G-rs8058823A in CD11a were significantly lower in BD patients. 25155097 2014