CYP2C18 c.819+2182G>A

Variant ID: 10-96468899-G-A

NM_000772.2(CYP2C18):c.819+2182G>A

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Distribution of a novel CYP2C haplotype in Native American populations.

Frontiers In Genetics
Fernandes, Vanessa Câmara VC; Pretti, Marco Antônio M MAM; Tsuneto, Luiza Tamie LT; Petzl-Erler, Maria Luiza ML; Suarez-Kurtz, Guilherme G
Publication Date: 2023

Variant appearance in text: rs11188059
PubMed Link: 37025454
Variant Present in the following documents:
  • Main text
  • fgene-14-1114742.pdf
View BVdb publication page



Editorial: Brief research reports in pharmacogenetics and pharmacogenomics: 2022.

Frontiers In Pharmacology
Sessa, Francesco F; Magdy, Tarek T; Sukasem, Chonlaphat C; Patrinos, George P GP
Publication Date: 2023

Variant appearance in text: rs11188059
PubMed Link: 36937855
Variant Present in the following documents:
  • fphar-14-1172265.pdf
View BVdb publication page



Epigenetic signatures in antidepressant treatment response: a methylome-wide association study in the EMC trial.

Translational Psychiatry
Engelmann, J J; Zillich, L L; Frank, J J; Wagner, S S; Cetin, M M; Herzog, D P DP; Müller, M B MB; Tadic, A A; Foo, J C JC; Sirignano, L L; Braus, D F DF; Dahmen, N N; Sordon, S S; Riemenschneider, M M; Spaniol, C C; Gasparoni, G G; Rietschel, M M; Witt, S H SH; Lieb, K K; Streit, F F
Publication Date: 2022-07-07

Variant appearance in text: rs11188059
PubMed Link: 35794104
Variant Present in the following documents:
  • Main text
  • 41398_2022_Article_2032.pdf
View BVdb publication page



Impact of the novel CYP2C:TG haplotype and CYP2B6 variants on sertraline exposure in a large patient population.

Clinical And Translational Science
Bråten, Line Skute LS; Ingelman-Sundberg, Magnus M; Jukic, Marin M MM; Molden, Espen E; Kringen, Marianne Kristiansen MK
Publication Date: 2022-09

Variant appearance in text: rs11188059
PubMed Link: 35668575
Variant Present in the following documents:
  • Main text
  • CTS-15-2135.pdf
View BVdb publication page



Omeprazole Treatment Failure in Gastroesophageal Reflux Disease and Genetic Variation at the CYP2C Locus.

Frontiers In Genetics
Kee, Ping Siu PS; Maggo, Simran D S SDS; Kennedy, Martin A MA; Barclay, Murray L ML; Miller, Allison L AL; Lehnert, Klaus K; Curtis, Maurice A MA; Faull, Richard L M RLM; Parker, Remai R; Chin, Paul K L PKL
Publication Date: 2022

Variant appearance in text: rs11188059
PubMed Link: 35664313
Variant Present in the following documents:
  • Main text
  • fgene-13-869160.pdf
View BVdb publication page



Analysis of pharmacogenetic traits in two distinct South African populations.

Human Genomics
Ikediobi, Ogechi O; Aouizerat, Bradley B; Xiao, Yuanyuan Y; Gandhi, Monica M; Gebhardt, Stefan S; Warnich, Louise L
Publication Date: 2011-05

Variant appearance in text: rs11188059
PubMed Link: 21712189
Variant Present in the following documents:
  • Main text
View BVdb publication page