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RS5569

  • Rs5569

    • 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

    Rs5569

    Rs5569

  • Norepinephrine transporter

    • Protein-coding gene in the species Homo sapiens

    implicated in both postural orthostatic tachycardia syndrome and panic disorder. rs5569 is a variant of SLC6A2. The norepinephrine transporter is composed of 12

    Norepinephrine transporter

    Norepinephrine transporter

    Norepinephrine_transporter

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RS5569