| SNP: rs4680 | |
|---|---|
| Name(s) | Val158Met, Val108/158Met, G1947A |
| Gene | COMT |
| Chromosome | 22 |
| Region | Exon 3 |
| External databases | |
| Ensembl | Human SNPView |
| dbSNP | 4680 |
| HapMap | 4680 |
| SNPedia | 4680 |
| AlzGene | Meta-analysis Overview |
| SzGene | Meta-analysis Overview |
In genetics, rs4680 (Val158Met) is a genetic variant. It is a single nucleotide polymorphism (SNP) in the COMT gene that codes catechol-O-Methyltransferase. The single nucleotide substitution between G--> A results in an amino acid change from valine to methionine at codon 158.
The A or Met allele is associated with lower enzymatic activity (due to thermoinstability), and with exploratory behaviour.
The polymorphism has been much studied in schizophrenia research but as of November 2011 meta-analysis in the SzGene database shows no or very little effect. [1]
Several personality genetics studies have examined the association of the polymorphism with personality traits including extroversion, risk aversion, and novelty seeking. [2] [3] [4] [5] [6]
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