Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Rs5569> ?p ?o. }
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- 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 wikiPageExternalLink carddisp.pl?gene=SLC6A2&search=neurodegenerative%20or%20senile&suff=txt&snp_show_mode=1&snp=224.
- Rs5569 wikiPageID "19428479".
- Rs5569 wikiPageRevisionID "594977896".
- Rs5569 gene "SLC6A2".
- Rs5569 hasPhotoCollection Rs5569.
- Rs5569 name "A1287G".
- Rs5569 name "G1287A".
- Rs5569 region "Exon 9".
- Rs5569 rsid "5569".
- Rs5569 subject Category:Single-nucleotide_polymorphisms.
- 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.".
- Rs5569 label "Rs5569".
- Rs5569 sameAs m.04m_gz7.
- Rs5569 sameAs Q7375574.
- Rs5569 sameAs Q7375574.
- Rs5569 wasDerivedFrom Rs5569?oldid=594977896.
- Rs5569 isPrimaryTopicOf Rs5569.