EDN1 c.533+356G>A

Variant ID: 6-12294993-G-A

NM_001955.4(EDN1):c.533+356G>A

This variant was identified in 12 publications

View GRCh38 version.




Publications:


Research status and prospects of biomarkers for nasopharyngeal carcinoma in the era of high‑throughput omics (Review).

International Journal Of Oncology
Zhang, Shan-Qiang SQ; Pan, Su-Ming SM; Liang, Si-Xian SX; Han, Yu-Shuai YS; Chen, Hai-Bin HB; Li, Ji-Cheng JC
Publication Date: 2021-04

Variant appearance in text: rs2071942
PubMed Link: 33649830
Variant Present in the following documents:
  • Main text
  • ijo-58-04-05188.pdf
View BVdb publication page



Association of +138I/D and Lys198Asn Polymorphisms in the Endothelin-1 Gene with Early Onset of Coronary Artery Disease among the Chinese Han Population.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Tu, Guosheng G; Fang, Zhengxu Z; Zhao, Yu Y; Wu, Qinghua Q
Publication Date: 2020-06-05

Variant appearance in text: rs2071942
PubMed Link: 32499477
Variant Present in the following documents:
  • Main text
  • medscimonit-26-e921542.pdf
View BVdb publication page



Endothelin-1 rs9296344 associates with the susceptibility of childhood primary nephrotic syndrome.

Journal Of Clinical Laboratory Analysis
Zhang, Ruifeng R; Yang, Huandan H; Zhu, Bingbing B; Yuan, Tingting T; Peng, Qianqian Q; Lv, Juan J; Qiu, Shan S; Zhou, Suqin S; Li, Yan Y; Zhong, Zhaowen Z
Publication Date: 2020-04

Variant appearance in text: rs2071942
PubMed Link: 31981468
Variant Present in the following documents:
  • Main text
  • JCLA-34-e23134.pdf
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Association of regenerating gene 1A single-nucleotide polymorphisms and nasopharyngeal carcinoma susceptibility in southern Chinese population.

European Archives Of Oto-Rhino-Laryngology : Official Journal Of The European Federation Of Oto-Rhino-Laryngological Societies (Eufos) : Affiliated With The German Society For Oto-Rhino-Laryngology - Head And Neck Surgery
Xing, Haijie H; Chen, Xiangdong X; Sun, Hongxia H; Han, Yaofeng Y; Ding, Lanshu L; Chen, Xiaoxia X
Publication Date: 2020-01

Variant appearance in text: rs2071942
PubMed Link: 31541294
Variant Present in the following documents:
  • Main text
  • 405_2019_Article_5645.pdf
View BVdb publication page



Polymorphism profiling of nine high altitude relevant candidate gene loci in acclimatized sojourners and adapted natives.

Bmc Genetics
Tomar, Arvind A; Malhotra, Seema S; Sarkar, Soma S
Publication Date: 2015-09-15

Variant appearance in text: rs2071942
PubMed Link: 26373931
Variant Present in the following documents:
  • Main text
View BVdb publication page



Primary biliary cirrhosis: From bench to bedside.

World Journal Of Gastrointestinal Pharmacology And Therapeutics
Kouroumalis, Elias E; Notas, George G
Publication Date: 2015-08-06

Variant appearance in text: rs2071942
PubMed Link: 26261733
Variant Present in the following documents:
  • Main text
View BVdb publication page



Patients with chronic three-vessel disease in a 15-year follow-up study: genetic and non-genetic predictors of survival.

Medicine
Máchal, Jan J; Pávková-Goldbergová, Monika M; Hlinomaz, Ota O; Groch, Ladislav L; Vašků, Anna A
Publication Date: 2014-12

Variant appearance in text: rs2071942
PubMed Link: 25526459
Variant Present in the following documents:
  • medi-93-e278.pdf
View BVdb publication page



Personalised medicine: not just in our genes.

Bmj (Clinical Research Ed.)
Kitsios, Georgios D GD; Kent, David M DM
Publication Date: 2012-04-03

Variant appearance in text: rs2071942
PubMed Link: 22491484
Variant Present in the following documents:
  • kitg001979.wt2_default.pdf
View BVdb publication page



Pharmacogenetics in chronic heart failure: new developments and current challenges.

Current Heart Failure Reports
Talameh, Jasmine A JA; Lanfear, David E DE
Publication Date: 2012-03

Variant appearance in text: rs2071942
PubMed Link: 22135185
Variant Present in the following documents:
  • Main text
View BVdb publication page



Unifying candidate gene and GWAS Approaches in Asthma.

Plos One
Michel, Sven S; Liang, Liming L; Depner, Martin M; Klopp, Norman N; Ruether, Andreas A; Kumar, Ashish A; Schedel, Michaela M; Vogelberg, Christian C; von Mutius, Erika E; von Berg, Andrea A; Bufe, Albrecht A; Rietschel, Ernst E; Heinzmann, Andrea A; Laub, Otto O; Simma, Burkhard B; Frischer, Thomas T; Genuneit, Jon J; Gut, Ivo G IG; Schreiber, Stefan S; Lathrop, Mark M; Illig, Thomas T; Kabesch, Michael M
Publication Date: 2010-11-12

Variant appearance in text: rs2071942
PubMed Link: 21103062
Variant Present in the following documents:
View BVdb publication page



Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.

The Journal Of Investigative Dermatology
Birlea, Stanca A SA; Jin, Ying Y; Bennett, Dorothy C DC; Herbstman, Deborah M DM; Wallace, Margaret R MR; McCormack, Wayne T WT; Kemp, E Helen EH; Gawkrodger, David J DJ; Weetman, Anthony P AP; Picardo, Mauro M; Leone, Giovanni G; Taïeb, Alain A; Jouary, Thomas T; Ezzedine, Khaled K; van Geel, Nanja N; Lambert, Jo J; Overbeck, Andreas A; Fain, Pamela R PR; Spritz, Richard A RA
Publication Date: 2011-02

Variant appearance in text: rs2071942
PubMed Link: 21085187
Variant Present in the following documents:
  • Main text
View BVdb publication page



Progress toward genetic tailoring of heart failure therapy.

Current Opinion In Molecular Therapeutics
Lillvis, John H JH; Lanfear, David E DE
Publication Date: 2010-06

Variant appearance in text: rs2071942
PubMed Link: 20521218
Variant Present in the following documents:
  • Main text
View BVdb publication page