NOS1 c.4289+720G>C

Variant ID: 12-117655131-C-G

NM_000620.4(NOS1):c.4289+720G>C

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis.

Frontiers In Pharmacology
Sales, Rahyssa Rodrigues RR; Nogueira, Bárbara Lisboa BL; Tosatti, Jéssica Abdo Gonçalves JAG; Gomes, Karina Braga KB; Luizon, Marcelo Rizzatti MR
Publication Date: 2021

Variant appearance in text: rs816361
PubMed Link: 35126118
Variant Present in the following documents:
  • Main text
  • fphar-12-779497.pdf
View BVdb publication page



Genome-based therapeutic interventions for β-type hemoglobinopathies.

Human Genomics
Karamperis, Kariofyllis K; Tsoumpeli, Maria T MT; Kounelis, Fotios F; Koromina, Maria M; Mitropoulou, Christina C; Moutinho, Catia C; Patrinos, George P GP
Publication Date: 2021-06-05

Variant appearance in text: rs816361
PubMed Link: 34090531
Variant Present in the following documents:
  • Main text
  • 40246_2021_Article_329.pdf
View BVdb publication page



Genetic Factors of Nitric Oxide's System in Psychoneurologic Disorders.

International Journal Of Molecular Sciences
Nasyrova, Regina F RF; Moskaleva, Polina V PV; Vaiman, Elena E EE; Shnayder, Natalya A NA; Blatt, Nataliya L NL; Rizvanov, Albert A AA
Publication Date: 2020-02-26

Variant appearance in text: rs816361
PubMed Link: 32111088
Variant Present in the following documents:
  • Main text
  • ijms-21-01604.pdf
View BVdb publication page



An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine.

Omics : A Journal Of Integrative Biology
Mnika, Khuthala K; Pule, Gift D GD; Dandara, Collet C; Wonkam, Ambroise A
Publication Date: 2016-10

Variant appearance in text: rs816361
PubMed Link: 27636225
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs816361
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page



Genetic polymorphisms in nitric oxide synthase genes modify the relationship between vegetable and fruit intake and risk of non-Hodgkin lymphoma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Han, Xuesong X; Zheng, Tongzhang T; Lan, Qing Q; Zhang, Yaqun Y; Kilfoy, Briseis A BA; Qin, Qin Q; Rothman, Nathaniel N; Zahm, Shelia H SH; Holford, Theodore R TR; Leaderer, Brian B; Zhang, Yawei Y
Publication Date: 2009-05

Variant appearance in text: rs816361
PubMed Link: 19423521
Variant Present in the following documents:
  • Main text
View BVdb publication page



IL10 polymorphisms are associated with airflow obstruction in severe alpha1-antitrypsin deficiency.

American Journal Of Respiratory Cell And Molecular Biology
Demeo, Dawn L DL; Campbell, Edward J EJ; Barker, Alan F AF; Brantly, Mark L ML; Eden, Edward E; McElvaney, N Gerard NG; Rennard, Stephen I SI; Sandhaus, Robert A RA; Stocks, James M JM; Stoller, James K JK; Strange, Charlie C; Turino, Gerard G; Silverman, Edwin K EK
Publication Date: 2008-01

Variant appearance in text: rs816361
PubMed Link: 17690329
Variant Present in the following documents:
  • Main text
View BVdb publication page