COMT c.1-303T>C

Variant ID: 22-19949747-T-C

NM_000754.3(COMT):c.1-303T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs11569716
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Catechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response.

The Pharmacogenomics Journal
Ji, Y Y; Biernacka, J J; Snyder, K K; Drews, M M; Pelleymounter, L L LL; Colby, C C; Wang, L L; Mrazek, D A DA; Weinshilboum, R M RM
Publication Date: 2012-02

Variant appearance in text: rs11569716
PubMed Link: 20877297
Variant Present in the following documents:
  • Main text
View BVdb publication page



Catechol O-methyltransferase pharmacogenomics: human liver genotype-phenotype correlation and proximal promoter studies.

Pharmacogenetics And Genomics
Zhang, Jianping J; Ji, Yuan Y; Moon, Irene I; Pelleymounter, Linda L LL; Ezequel Salavaggione, Oreste O; Wu, Yanhong Y; Jenkins, Gregory D GD; Batzler, Anthony J AJ; Schaid, Daniel J DJ; Weinshilboum, Richard M RM
Publication Date: 2009-08

Variant appearance in text: rs11569716
PubMed Link: 19641441
Variant Present in the following documents:
  • Main text
View BVdb publication page