Reference for RS6313. Search for RS6313

AI searches containing RS6313

RS6313

Rs6313

Single nucleotide polymorphism in human HTR2A gene

In genetics, rs6313 also called T102C or C102T is a gene variation—a single nucleotide polymorphism (SNP)—in the human HTR2A gene that codes for the 5-HT2A

Rs6313

Rs6311

people with the A-allele may have slightly elevated risk of schizophrenia. rs6313, rs6314, and rs7997012 are other investigated SNPs in the HTR2A gene. Ham

Rs6311

5-HT2A receptor

Subtype of serotonin receptor

polymorphisms have been identified for HTR2A: A-1438G (rs6311), C102T (rs6313), and His452Tyr (rs6314). Many more polymorphisms exist for the gene. A

5-HT2A receptor

5-HT2A_receptor

Rs6314

another group. The His452Tyr variant may influence cell signaling. rs6311, rs6313 and rs7997012 are other investigated SNPs in the HTR2A gene. "SNP linked

Rs6314

Rs7997012

associated with either major depressive disorder or bipolar disorder. Rs6311, rs6313 and His452Tyr (rs6314) are other SNPs in the HTR2A gene. There are many

Rs7997012

Sport psychology

Branch of psychology

with athletic performance outcomes is the HTR2A gene, specifically the rs6313 variant. HTR2A is responsible for encoding the serotonin 2A receptor, which

Sport psychology

Sport_psychology

Single-nucleotide polymorphism

Single nucleotide in genomic DNA at which different sequence alternatives exist

play an important role in disease initiation and progression. rs6311 and rs6313 are SNPs in the Serotonin 5-HT2A receptor gene on human chromosome 13. The

Single-nucleotide polymorphism

Single-nucleotide_polymorphism

Psychiatric genetics

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

allele), NPSR1 (rs324981, T allele), TPH1 (rs1800532, AA genotype), HTR2A (rs6313, T allele), and MAOA (uVNTR, long alleles) genes to be involved through

Psychiatric genetics

Psychiatric_genetics