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About: Rs6313     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : yago:SingleNucleotidePolymorphism111493452, within Data Space : dbpedia.org:8891 associated with source document(s)

Type: workyago:WikicatSingle-nucleotidePolymorphismsyago:NaturalPhenomenon111408559yago:OrganicPhenomenon111418750yago:Phenomenon100034213yago:PhysicalEntity100001930yago:Polymorphism111493266yago:Process100029677yago:SingleNucleotidePolymorphism111493452 New Facet based on Instances of this Class

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 receptor.The SNP is a synonymous substitution located in exon 1 of the gene where it is involved in coding the 34th amino acid as serine. Meta-analyses seem to indicate that the SNP is not directly associated with schizophrenia,not with Alzheimer's disease,and two initial studies seem to indicate that it is not associated with Parkinson's disease.