COMT c.-92+3628T>G

Variant ID: 22-19933048-T-G

NM_000754.4(COMT):c.-92+3628T>G

This variant was identified in 4 publications

View GRCh38 version.




Publications:


A common polymorphism of COMT was associated with symptomatic lumbar disc herniation based on a large sample with Chinese Han ancestry.

Scientific Reports
Liu, Hongliang H; Zhao, Hongmou H; Li, Zhong Z; Xue, Hanzhong H; Lu, Jun J; Ma, Wei W
Publication Date: 2018-08-29

Variant appearance in text: rs8185002
PubMed Link: 30158547
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_31240.pdf
View BVdb publication page



Predictors of Neurocognitive Syndromes in Combat Veterans.

Cureus
Roy, Michael J MJ; Costanzo, Michelle M; Gill, Jessica J; Leaman, Suzanne S; Law, Wendy W; Ndiongue, Rochelle R; Taylor, Patricia P; Kim, Hyung-Suk HS; Bieler, Gayle S GS; Garge, Nikhil N; Rapp, Paul E PE; Keyser, David D; Nathan, Dominic D; Xydakis, Michael M; Pham, Dzung D; Wassermann, Eric E
Publication Date: 2015-07

Variant appearance in text: rs8185002
PubMed Link: 26251769
Variant Present in the following documents:
  • Main text
  • cureus-0007-000000000293.pdf
View BVdb publication page



The genetic interacting landscape of 63 candidate genes in Major Depressive Disorder: an explorative study.

Biodata Mining
Lekman, Magnus M; Hössjer, Ola O; Andrews, Peter P; Källberg, Henrik H; Uvehag, Daniel D; Charney, Dennis D; Manji, Husseini H; Rush, John A JA; McMahon, Francis J FJ; Moore, Jason H JH; Kockum, Ingrid I
Publication Date: 2014

Variant appearance in text: rs8185002
PubMed Link: 25279001
Variant Present in the following documents:
  • Main text
  • 1756-0381-7-19.pdf
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: rs8185002
PubMed Link: 24343288
Variant Present in the following documents:
  • Main text
View BVdb publication page