SLC6A4, solute carrier family 6 member 4, 6532

N. diseases: 440; N. variants: 28
Disease: Alexithymia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002020
Disease: Alexithymia
Alexithymia 		0.050 GeneticVariation phenotype BEFREE The findings suggest that the 5-HTTLPR and COMT Val158Met polymorphisms are not associated with alexithymia. 30707988 2019
CUI: C0002020
Disease: Alexithymia
Alexithymia 		0.050 GeneticVariation phenotype BEFREE We measured IL-18 serum levels in 115 Italian-Caucasian healthy subjects genotyped for 5-HTTLPR allele variants, divided by gender and assessed for alexithymia scores using the 20-item Toronto Alexithymia Scale. 30326484 2018
CUI: C0002020
Disease: Alexithymia
Alexithymia 		0.050 GeneticVariation phenotype BEFREE Patients with homozygosity for HTR1A-G and 5-HTTLPR long alleles had significantly higher levels of alexithymia. 26609890 2015
CUI: C0002020
Disease: Alexithymia
Alexithymia 		0.050 GeneticVariation phenotype BEFREE We investigated the possibility that polymorphism of the 5-HT transporter-linked promoter region (5-HTTLPR) is associated with alexithymia. 22222552 2012
CUI: C0002020
Disease: Alexithymia
Alexithymia 		0.050 GeneticVariation phenotype BEFREE We investigated the relationship between COMT Val108/158Met, serotonin transporter coding sequence (5-HT transporter gene-linked polymorphic region; 5-HTTLPR) polymorphisms, and alexithymia. 16127282 2005