Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Gilles de la Tourette syndrome
CUI: C0040517
Disease: Gilles de la Tourette syndrome
0.010 GeneticVariation BEFREE Compared with the published CNR1 sequence, three single base substitutions were identified: 1326T --> A, 1359G --> A, 1419 + 1G --> C. The change at position 1359 is a common polymorphism (1359 G/A) without allelic association with TS. 15108190 2004