DBH c.339+109G>C

Variant ID: 9-136501941-G-C

NM_000787.3(DBH):c.339+109G>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Association of regulatory variants of dopamine β-hydroxylase with cognition and tardive dyskinesia in schizophrenia subjects.

Journal Of Psychopharmacology (Oxford, England)
Punchaichira, Toyanji J TJ; Mukhopadhyay, Anirban A; Kukshal, Prachi P; Bhatia, Triptish T; Deshpande, Smita N SN; Thelma, B K BK
Publication Date: 2020-03

Variant appearance in text: rs2797849
PubMed Link: 31913053
Variant Present in the following documents:
  • Main text
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs2797849
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 2
View BVdb publication page



Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12

Variant appearance in text: rs2797849
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
View BVdb publication page



Epistasis between neurochemical gene polymorphisms and risk for ADHD.

European Journal Of Human Genetics : Ejhg
Segurado, Ricardo R; Bellgrove, Mark A MA; Manconi, Francesca F; Gill, Michael M; Hawi, Ziarah Z
Publication Date: 2011-05

Variant appearance in text: rs2797849
PubMed Link: 21368917
Variant Present in the following documents:
  • Main text
View BVdb publication page



Human dopamine β-hydroxylase promoter variant alters transcription in chromaffin cells, enzyme secretion, and blood pressure.

American Journal Of Hypertension
Chen, Yuqing Y; Zhang, Kuixing K; Wen, Gen G; Rao, Fangwen F; Sanchez, Amber P AP; Wang, Lei L; Rodriguez-Flores, Juan L JL; Mahata, Manjula M; Mahata, Sushil K SK; Waalen, Jill J; Ziegler, Michael G MG; Hamilton, Bruce A BA; O'Connor, Daniel T DT
Publication Date: 2011-01

Variant appearance in text: rs2797849
PubMed Link: 20814407
Variant Present in the following documents:
  • Main text
View BVdb publication page



SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Kollins, S H SH; Anastopoulos, A D AD; Lachiewicz, A M AM; FitzGerald, D D; Morrissey-Kane, E E; Garrett, M E ME; Keatts, S L SL; Ashley-Koch, A E AE
Publication Date: 2008-12-05

Variant appearance in text: rs2797849
PubMed Link: 18821566
Variant Present in the following documents:
  • Main text
View BVdb publication page