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Rs1800532

Index Rs1800532

In genetics, rs1800532 (A218C) is a genetic variant. [1]

9 relations: Gene, Genetics, Intron, Neuropsychobiology, Peter Singer, Rs1799913, Single-nucleotide polymorphism, TPH1, Trait theory.

Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

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Genetics

Genetics is the study of genes, genetic variation, and heredity in living organisms.

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Intron

An intron is any nucleotide sequence within a gene that is removed by RNA splicing during maturation of the final RNA product.

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Neuropsychobiology

Neuropsychobiology is a peer-reviewed scientific journal that focuses on neuroscience, psychopharmacology, and biological psychiatry.

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Peter Singer

Peter Albert David Singer, AC (born 6 July 1946) is an Australian moral philosopher.

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Rs1799913

In genetics, rs1799913, also called A779C, is a gene variation—a single nucleotide polymorphism (SNP)— in the TPH1 gene.

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Single-nucleotide polymorphism

A single-nucleotide polymorphism, often abbreviated to SNP (plural), is a variation in a single nucleotide that occurs at a specific position in the genome, where each variation is present to some appreciable degree within a population (e.g. > 1%).

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TPH1

Tryptophan hydroxylase 1 (TPH1) is an isoenzyme of tryptophan hydroxylase which in humans is encoded by the TPH1 gene.

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Trait theory

In psychology, trait theory (also called dispositional theory) is an approach to the study of human personality.

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A218C.

References

[1] https://en.wikipedia.org/wiki/Rs1800532

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