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RS1800532

  • Rs1800532
  • In genetics, rs1800532 (A218C) is a genetic variant. It is a single nucleotide polymorphism in the TPH1 gene and located in intron 7. It has been examined

    Rs1800532

    Rs1800532

  • Rs1799913
  • addiction. Other study relate it to figural and numeric creativity. A218C (rs1800532) is another SNP in the same intron in the same gene. D. A. Nielsen, G

    Rs1799913

    Rs1799913

  • Psychiatric genetics
  • Research field focused on role of genetics in development of mental disorders

    the COMT (rs4680, G [val] allele), NPSR1 (rs324981, T allele), TPH1 (rs1800532, AA genotype), HTR2A (rs6313, T allele), and MAOA (uVNTR, long alleles)

    Psychiatric genetics

    Psychiatric_genetics

  • TPH1
  • Protein-coding gene in the species Homo sapiens

    TPH2 Rs1799913 (A779C): intron related to figural and numeric creativity rs1800532 (A218C) GRCh38: Ensembl release 89: ENSG00000129167 – Ensembl, May 2017

    TPH1

    TPH1

    TPH1

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