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About: Rs5569     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : yago:SingleNucleotidePolymorphism111493452, within Data Space : dbpedia.org:8891 associated with source document(s)

Type: yago:WikicatSingle-nucleotidePolymorphismsyago:NaturalPhenomenon111408559yago:OrganicPhenomenon111418750yago:Phenomenon100034213yago:PhysicalEntity100001930yago:Polymorphism111493266yago:Process100029677yago:SingleNucleotidePolymorphism111493452 New Facet based on Instances of this Class

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.