SLC19A1, solute carrier family 19 member 1, 6573

N. diseases: 28; N. variants: 16
Disease: Autistic Disorder ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.310 Biomarker disease CTD_human A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism. 20468076 2010
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.310 Biomarker disease CTD_human Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism. 16917939 2006