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In genetics, rs7997012 is a gene variation—a single nucleotide polymorphism (SNP)—in intron 2 of the human HTR2A gene that codes for the 5-HT2A receptor
Rs7997012
Single nucleotide polymorphism in human HTR2A gene
with the rs6311 (A-1438G). A less well investigated SNP of this gene is rs7997012. Meta-analyses seem to indicate that the SNP is directly associated with
Rs6313
Nonspecific long-lasting anxiety
Variants in the gene encoding serotonin receptor 2A, HTR2A, particularly the rs7997012 SNP G allele, have been implicated in reductions in anxiety symptoms after
Generalized_anxiety_disorder
may have slightly elevated risk of schizophrenia. rs6313, rs6314, and rs7997012 are other investigated SNPs in the HTR2A gene. Ham BJ, Kim YH, Choi MJ
Rs6311
The His452Tyr variant may influence cell signaling. rs6311, rs6313 and rs7997012 are other investigated SNPs in the HTR2A gene. "SNP linked to Gene HTR2A"
Rs6314
RS7997012
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RS7997012