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SNP information rs4565946

RS4565946

Normal allele: CC

Polymorphism rs4565946 is related to topics like this:

Serotonin transporter sert

In humans, the SLC6A4 gene encodes a protein referred to as both the sodium-dependent serotonin...

Is OCD obsessive compulsive disorder genetic

Obsessive-compulsive disorder (OCD) is a mental health condition characterized by features known as...


Research and publications:

  16116490   Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.

  16146581   Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder.

  17346350   Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.

  19800079   Association of polymorphisms of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior.

  20159345   Molecular genetics of attention deficit hyperactivity disorder.

  20403506   Genetic variation in neuroendocrine genes associates with somatic symptoms in the general population: results from the EPIFUND study.

  21085052   Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity.

  21333900   The role of genetics in IBS

  21655053   The genetic basis of panic disorder.

  21873838   Association between tryptophan hydroxylase-2 gene and late-onset depression.

  22655589   Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics.

  22835848   Tryptophan hydroxylase 2 gene polymorphisms and poststroke anxiety disorders.

  23970845   The Genetics of Obsessive-Compulsive Disorder.

  27462201   From Genetics to Epigenetics: New Perspectives in Tourette Syndrome Research.

  27871272   Association of tryptophan hydroxylase-2 polymorphisms with oppositional defiant disorder in a Chinese Han population.

  28555406   Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.

CYP21 deficiency

The inability to synthesize cortisol, known as congenital adrenal hyperplasia (CAH), is responsible...

Dopamine transporter genes

The membrane-bound protein called the dopamine transporter (DAT), also known as the...

Mitochondria dna

The mitochondria contain circular chromosomes known as mitochondrial DNA and are organelles...

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