RYR3 c.1573+431T>G

Variant ID: 15-33874275-T-G

NM_001036.3(RYR3):c.1573+431T>G

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Calcium-channel blockers: Clinical outcome associations with reported pharmacogenetics variants in 32 000 patients.

British Journal Of Clinical Pharmacology
Türkmen, Deniz D; Masoli, Jane A H JAH; Delgado, João J; Kuo, Chia-Ling CL; Bowden, Jack J; Melzer, David D; Pilling, Luke C LC
Publication Date: 2022-09-22

Variant appearance in text: rs877087
PubMed Link: 36134646
Variant Present in the following documents:
  • Main text
  • BCP-89-853.pdf
View BVdb publication page



Pharmacogenomics of amlodipine and hydrochlorothiazide therapy and the quest for improved control of hypertension: a mini review.

Heart Failure Reviews
Johnson, Rabia R; Dludla, Phiwayinkosi P; Mabhida, Sihle S; Benjeddou, Mongi M; Louw, Johan J; February, Faghri F
Publication Date: 2019-05

Variant appearance in text: rs877087
PubMed Link: 30645721
Variant Present in the following documents:
  • Main text
  • 10741_2018_Article_9765.pdf
View BVdb publication page



Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population.

Bmc Cardiovascular Disorders
Zhao, Chenxi C; Ikeda, Shinobu S; Arai, Tomio T; Naka-Mieno, Makiko M; Sato, Noriko N; Muramatsu, Masaaki M; Sawabe, Motoji M
Publication Date: 2014-01-14

Variant appearance in text: rs877087
PubMed Link: 24423397
Variant Present in the following documents:
  • Main text
  • 1471-2261-14-6.pdf
View BVdb publication page



RYR3 gene polymorphisms and cardiovascular disease outcomes in the context of antihypertensive treatment.

The Pharmacogenomics Journal
Lynch, A I AI; Irvin, M R MR; Boerwinkle, E E; Davis, B R BR; Vaughan, L K LK; Ford, C E CE; Aissani, B B; Eckfeldt, J H JH; Arnett, D K DK; Shrestha, S S
Publication Date: 2013-08

Variant appearance in text: rs877087
PubMed Link: 22664477
Variant Present in the following documents:
  • Main text
  • nihms374192.pdf
View BVdb publication page



Genomewide association studies of stroke.

The New England Journal Of Medicine
Ikram, M Arfan MA; Seshadri, Sudha S; Bis, Joshua C JC; Fornage, Myriam M; DeStefano, Anita L AL; Aulchenko, Yurii S YS; Debette, Stephanie S; Lumley, Thomas T; Folsom, Aaron R AR; van den Herik, Evita G EG; Bos, Michiel J MJ; Beiser, Alexa A; Cushman, Mary M; Launer, Lenore J LJ; Shahar, Eyal E; Struchalin, Maksim M; Du, Yangchun Y; Glazer, Nicole L NL; Rosamond, Wayne D WD; Rivadeneira, Fernando F; Kelly-Hayes, Margaret M; Lopez, Oscar L OL; Coresh, Josef J; Hofman, Albert A; DeCarli, Charles C; Heckbert, Susan R SR; Koudstaal, Peter J PJ; Yang, Qiong Q; Smith, Nicholas L NL; Kase, Carlos S CS; Rice, Kenneth K; Haritunians, Talin T; Roks, Gerwin G; de Kort, Paul L M PL; Taylor, Kent D KD; de Lau, Lonneke M LM; Oostra, Ben A BA; Uitterlinden, Andre G AG; Rotter, Jerome I JI; Boerwinkle, Eric E; Psaty, Bruce M BM; Mosley, Thomas H TH; van Duijn, Cornelia M CM; Breteler, Monique M B MM; Longstreth, W T WT; Wolf, Philip A PA
Publication Date: 2009-04-23

Variant appearance in text: rs877087
PubMed Link: 19369658
Variant Present in the following documents:
  • Main text
View BVdb publication page