SLC5A7, solute carrier family 5 member 7, 60482

N. diseases: 127; N. variants: 12
Disease: Gilles de la Tourette syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1013940
rs1013940
Entrez Id: 60482
Gene Symbol: SLC5A7
SLC5A7
CUI: C0040517
Disease:
Gilles de la Tourette syndrome 		0.010 GeneticVariation BEFREE To investigate the association between the SLC5A7 polymorphisms and Tourette syndrome (TS) in the Chinese Han population, the SNP rs1013940, rs2433718, and rs4676169 were genotyped in 401 TS trios and 400 controls. 28830823 2017
dbSNP: rs2433718
rs2433718
Entrez Id: 60482
Gene Symbol: SLC5A7
SLC5A7
CUI: C0040517
Disease:
Gilles de la Tourette syndrome 		0.010 GeneticVariation BEFREE To investigate the association between the SLC5A7 polymorphisms and Tourette syndrome (TS) in the Chinese Han population, the SNP rs1013940, rs2433718, and rs4676169 were genotyped in 401 TS trios and 400 controls. 28830823 2017
dbSNP: rs4676169
rs4676169
Entrez Id: 60482
Gene Symbol: SLC5A7
SLC5A7
CUI: C0040517
Disease:
Gilles de la Tourette syndrome 		0.010 GeneticVariation BEFREE To investigate the association between the SLC5A7 polymorphisms and Tourette syndrome (TS) in the Chinese Han population, the SNP rs1013940, rs2433718, and rs4676169 were genotyped in 401 TS trios and 400 controls. 28830823 2017