Matches in DBpedia 2014 for { ?s ?p In genetics, rs5569 (A1287G or G1287A) is a genetic variant.It is a single nucleotide polymorphism (SNP) in the SLC6A2 gene in exon 9.This gene codes the norepinephrine transporter.The SNP is a silent substitution andthe nucleotides of both variants code a threonine amino acid.Several research studies have examined the effect of the variant in relation to alcohol dependence,attention deficit hyperactivity disorder,diabetes,major depressive disorder,panic disorder,Tourette syndromeand personality traits.None of the studies have found an association.. }
Showing items 1 to 2 of
2
with 100 items per page.
- Rs5569 abstract "In genetics, rs5569 (A1287G or G1287A) is a genetic variant.It is a single nucleotide polymorphism (SNP) in the SLC6A2 gene in exon 9.This gene codes the norepinephrine transporter.The SNP is a silent substitution andthe nucleotides of both variants code a threonine amino acid.Several research studies have examined the effect of the variant in relation to alcohol dependence,attention deficit hyperactivity disorder,diabetes,major depressive disorder,panic disorder,Tourette syndromeand personality traits.None of the studies have found an association.".
- Rs5569 comment "In genetics, rs5569 (A1287G or G1287A) is a genetic variant.It is a single nucleotide polymorphism (SNP) in the SLC6A2 gene in exon 9.This gene codes the norepinephrine transporter.The SNP is a silent substitution andthe nucleotides of both variants code a threonine amino acid.Several research studies have examined the effect of the variant in relation to alcohol dependence,attention deficit hyperactivity disorder,diabetes,major depressive disorder,panic disorder,Tourette syndromeand personality traits.None of the studies have found an association.".