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Rs1799913

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In genetics, rs1799913, also called A779C, is a gene variation—a single nucleotide polymorphism (SNP)— in the TPH1 gene. [1]

11 relations: Behavior Genetics (journal), Gene, Human Genetics (journal), Intron, Mary Jeanne Kreek, Molecular Brain Research, Opioid use disorder, Rs1800532, Schizophrenia, Single-nucleotide polymorphism, TPH1.

Behavior Genetics (journal)

Behavior Genetics is a peer-reviewed scientific journal published monthly by Springer Science+Business Media that is covering "research in the inheritance of behavior".

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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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Human Genetics (journal)

Human Genetics is a peer-reviewed medical journal covering all aspects of human genetics, including legal and social issues.

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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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Mary Jeanne Kreek

Mary Jeanne Kreek (born 1937) is an American neurobiologist specializing in the study and treatment of addiction.

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Molecular Brain Research

Molecular Brain Research was a peer-reviewed scientific journal of molecular neuroscience.

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Opioid use disorder

Opioid use disorder is a medical condition characterized by a problematic pattern of opioid use that causes clinically significant impairment or distress.

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Rs1800532

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

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Schizophrenia

Schizophrenia is a mental disorder characterized by abnormal social behavior and failure to understand reality.

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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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A779C.

References

[1] https://en.wikipedia.org/wiki/Rs1799913

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