Annotation Detail
Information
- Associated Genes
- SLC6A2
- Associated Variants
-
SLC6A2 MUTATION
SLC6A2 MUTATION
SLC6A2 p.Thr429= (p.T429=) ( ENST00000567238.1, ENST00000568943.6, ENST00000561820.5, ENST00000219833.13, ENST00000566163.5, ENST00000414754.7, ENST00000379906.6 )
SLC6A2 p.Thr429= (p.T429=) ( ENST00000566163.5, ENST00000219833.13, ENST00000414754.7, ENST00000379906.6, ENST00000567238.1, ENST00000561820.5, ENST00000568943.6 )
SLC6A2 p.Thr429= (p.T429=) ( ENST00000219833.13, ENST00000379906.6, ENST00000414754.7, ENST00000561820.5, ENST00000566163.5, ENST00000567238.1, ENST00000568943.6 )
SLC6A2 p.Thr429= (p.T429=) ( ENST00000219833.13, ENST00000379906.6, ENST00000414754.7, ENST00000561820.5, ENST00000566163.5, ENST00000567238.1, ENST00000568943.6 ) - Associated Disease
- attention deficit hyperactivity disorder
- Source Database
- DisGeNET
- Description
- The 1287 G/A polymorphism of the norepinephrine transporter gene (NET) is involved in commission errors in Korean children with attention deficit hyperactivity disorder.
- Pubmed
- 21569456
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.0431817969673997
- Year of publication
- 2011
Drugs