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In genetics, rs6311 is a gene variation—a single nucleotide polymorphism (SNP)—in the human HTR2A gene that codes for the 5-HT2A receptor. 5-HT2A is a
Rs6311
Single nucleotide polymorphism in human HTR2A gene
attention: rs6311 and His452Tyr (rs6314). The T102C polymorphism has been shown to be in complete linkage disequilibrium with the rs6311 (A-1438G). A
Rs6313
not associated with either major depressive disorder or bipolar disorder. Rs6311, rs6313 and His452Tyr (rs6314) are other SNPs in the HTR2A gene. There are
Rs7997012
Single nucleotide in genomic DNA at which different sequence alternatives exist
interaction also play an important role in disease initiation and progression. rs6311 and rs6313 are SNPs in the Serotonin 5-HT2A receptor gene on human chromosome
Single-nucleotide polymorphism
Single-nucleotide_polymorphism
Subtype of serotonin receptor
Several interesting polymorphisms have been identified for HTR2A: A-1438G (rs6311), C102T (rs6313), and His452Tyr (rs6314). Many more polymorphisms exist
5-HT2A_receptor
replicated by another group. The His452Tyr variant may influence cell signaling. rs6311, rs6313 and rs7997012 are other investigated SNPs in the HTR2A gene. "SNP
Rs6314
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