About: Rs1800532

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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 in relation to personality traits. A779C is another SNP in same intron.

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  • 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 in relation to personality traits. A779C is another SNP in same intron. (en)
  • Rs1800532 (A218C) — однонуклеотидный полиморфизм, расположенный в 7 интроне гена TPH1, кодирующего триптофангидроксилазу. Исследования связывают этот полиморфизм с особенностями характера. Ещё один исследуемый SNP в том же интроне — A779C. (ru)
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  • 19438297 (xsd:integer)
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  • 1925 (xsd:nonNegativeInteger)
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  • 994519460 (xsd:integer)
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dbp:chromosome
  • 11 (xsd:integer)
dbp:gene
  • TPH1 (en)
dbp:name
  • A218C (en)
dbp:region
  • Intron 7 (en)
dbp:rsid
  • 1800532 (xsd:integer)
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gold:hypernym
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rdfs:comment
  • 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 in relation to personality traits. A779C is another SNP in same intron. (en)
  • Rs1800532 (A218C) — однонуклеотидный полиморфизм, расположенный в 7 интроне гена TPH1, кодирующего триптофангидроксилазу. Исследования связывают этот полиморфизм с особенностями характера. Ещё один исследуемый SNP в том же интроне — A779C. (ru)
rdfs:label
  • Rs1800532 (en)
  • Rs1800532 (ru)
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