COMT c.616-902G>T

Variant ID: 22-19955157-G-T

NM_000754.3(COMT):c.616-902G>T

This variant was identified in 4 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: rs9306235
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



A genome-wide association study of clinical symptoms of dissociation in a trauma-exposed sample.

Depression And Anxiety
Wolf, Erika J EJ; Rasmusson, Ann M AM; Mitchell, Karen S KS; Logue, Mark W MW; Baldwin, Clinton T CT; Miller, Mark W MW
Publication Date: 2014-04

Variant appearance in text: rs9306235
PubMed Link: 24677629
Variant Present in the following documents:
  • Main text
View BVdb publication page



Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer.

Anesthesiology
Kambur, Oleg O; Kaunisto, Mari A MA; Tikkanen, Emmi E; Leal, Suzanne M SM; Ripatti, Samuli S; Kalso, Eija A EA
Publication Date: 2013-12

Variant appearance in text: rs9306235
PubMed Link: 24343288
Variant Present in the following documents:
  • Main text
View BVdb publication page



Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models.

Human Heredity
Fridley, Brooke L BL; Jenkins, Gregory D GD
Publication Date: 2010

Variant appearance in text: rs9306235
PubMed Link: 20551675
Variant Present in the following documents:
  • Main text
View BVdb publication page