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OverviewHigh Quality Content by WIKIPEDIA articles! 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. The SNP varies between adenine (A) and guanine (G) DNA bases with the G-allele being most frequent. A research study found it to be related to antidepressant treatment. The research group reported that a polymorphism (rs1954787) on another gene, the GRIK4, has also shown a treatment-response-association in this kind of treatment. In a Japanese study rs7997012 was not associated with neither major depressive disorder nor bipolar disorder. Rs6311, rs6313 and His452Tyr (rs6314) are other SNPs in the HTR2A gene. There are many more, even in intron 2 alone. Full Product DetailsAuthor: Lambert M. Surhone , Miriam T. Timpledon , Susan F. MarsekenPublisher: VDM Publishing House Imprint: VDM Publishing House Dimensions: Width: 22.90cm , Height: 0.60cm , Length: 15.20cm Weight: 0.176kg ISBN: 9786130594077ISBN 10: 6130594070 Pages: 112 Publication Date: 04 July 2010 Audience: General/trade , General Format: Paperback Publisher's Status: Active Availability: In Print  This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
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