COMT c.-92+5579T>C

Variant ID: 22-19934999-T-C

NM_000754.4(COMT):c.-92+5579T>C

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Pain polymorphisms and opioids: An evidence based review.

Molecular Medicine Reports
Vieira, Cláudia Margarida Pereira CMP; Fragoso, Rosa Maria RM; Pereira, Deolinda D; Medeiros, Rui R
Publication Date: 2019-03

Variant appearance in text: rs174680
PubMed Link: 30592275
Variant Present in the following documents:
  • Main text
  • mmr-19-03-1423.pdf
View BVdb publication page



Neurocognitive Functioning of Children Treated for High-Risk B-Acute Lymphoblastic Leukemia Randomly Assigned to Different Methotrexate and Corticosteroid Treatment Strategies: A Report From the Children's Oncology Group.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Hardy, Kristina K KK; Embry, Leanne L; Kairalla, John A JA; Helian, Shanjun S; Devidas, Meenakshi M; Armstrong, Daniel D; Hunger, Stephen S; Carroll, William L WL; Larsen, Eric E; Raetz, Elizabeth A EA; Loh, Mignon L ML; Yang, Wenjian W; Relling, Mary V MV; Noll, Robert B RB; Winick, Naomi N
Publication Date: 2017-08-10

Variant appearance in text: rs174680
PubMed Link: 28671857
Variant Present in the following documents:
  • Main text
View BVdb publication page



Is ethnicity associated with morphine's side effects in children? Morphine pharmacokinetics, analgesic response, and side effects in children having tonsillectomy.

Paediatric Anaesthesia
Jimenez, Nathalia N; Anderson, Gail D GD; Shen, Danny D DD; Nielsen, Susan S SS; Farin, Federico M FM; Seidel, Kristy K; Lynn, Anne M AM
Publication Date: 2012-07

Variant appearance in text: rs174680
PubMed Link: 22486937
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.

Molecular Pain
Rakvåg, Trude T TT; Ross, Joy R JR; Sato, Hiroe H; Skorpen, Frank F; Kaasa, Stein S; Klepstad, Pål P
Publication Date: 2008-12-18

Variant appearance in text: rs174680
PubMed Link: 19094200
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.

Bmc Medicine
Van Ness, Brian B; Ramos, Christine C; Haznadar, Majda M; Hoering, Antje A; Haessler, Jeff J; Crowley, John J; Jacobus, Susanna S; Oken, Martin M; Rajkumar, Vincent V; Greipp, Philip P; Barlogie, Bart B; Durie, Brian B; Katz, Michael M; Atluri, Gowtham G; Fang, Gang G; Gupta, Rohit R; Steinbach, Michael M; Kumar, Vipin V; Mushlin, Richard R; Johnson, David D; Morgan, Gareth G
Publication Date: 2008-09-08

Variant appearance in text: rs174680
PubMed Link: 18778477
Variant Present in the following documents:
  • Main text
  • 1741-7015-6-26.pdf
View BVdb publication page