NOS3 c.1753-1083A>T

Variant ID: 7-150702432-A-T

NM_000603.4(NOS3):c.1753-1083A>T

This variant was identified in 13 publications

View GRCh38 version.




Publications:


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: rs3918186
PubMed Link: 32111088
Variant Present in the following documents:
  • Main text
  • ijms-21-01604.pdf
View BVdb publication page



Endothelial nitric oxide gene polymorphisms and their association with coronary artery disease in Tunisian population.

Anatolian Journal Of Cardiology
Afef, Letaief L; Leila, Benothmane B; Bassem, Charfeddine C; Samia, Ernez Hajri EH; Jridi, Guider G; Khalifa, Limem L
Publication Date: 2017-01

Variant appearance in text: rs3918186
PubMed Link: 27443477
Variant Present in the following documents:
  • Main text
  • AJC-17-31.pdf
View BVdb publication page



Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study.

Environmental Health Perspectives
Wu, Fen F; Jasmine, Farzana F; Kibriya, Muhammad G MG; Liu, Mengling M; Cheng, Xin X; Parvez, Faruque F; Islam, Tariqul T; Ahmed, Alauddin A; Rakibuz-Zaman, Muhammad M; Jiang, Jieying J; Roy, Shantanu S; Paul-Brutus, Rachelle R; Slavkovich, Vesna V; Islam, Tariqul T; Levy, Diane D; VanderWeele, Tyler J TJ; Pierce, Brandon L BL; Graziano, Joseph H JH; Ahsan, Habibul H; Chen, Yu Y
Publication Date: 2015-05

Variant appearance in text: rs3918186
PubMed Link: 25575156
Variant Present in the following documents:
  • ehp.1307883.s001.508.pdf
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Association of NOS3 gene variants and clinical contributors of hypoxic-ischemic encephalopathy.

Brazilian Journal Of Medical And Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
Kuzmanić Šamija, R R; Primorac, D D; Rešić, B B; Pavlov, V V; Čapkun, V V; Punda, H H; Lozić, B B; Zemunik, T T
Publication Date: 2014-10

Variant appearance in text: rs3918186
PubMed Link: 25140814
Variant Present in the following documents:
  • Main text
  • 1414-431X-bjmbr-47-10-00869.pdf
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Single nucleotide polymorphism-single nucleotide polymorphism interactions among inflammation genes in the genetic architecture of blood pressure in the Framingham Heart Study.

American Journal Of Hypertension
Basson, Jacob J JJ; de Las Fuentes, Lisa L; Rao, Dabeeru C DC
Publication Date: 2015-02

Variant appearance in text: rs3918186
PubMed Link: 25063733
Variant Present in the following documents:
  • Main text
View BVdb publication page



Using a Bayesian hierarchical model for identifying single nucleotide polymorphisms associated with childhood acute lymphoblastic leukemia risk in case-parent triads.

Plos One
Cao, Ying Y; Lupo, Philip J PJ; Swartz, Michael D MD; Nousome, Darryl D; Scheurer, Michael E ME
Publication Date: 2013

Variant appearance in text: rs3918186
PubMed Link: 24367687
Variant Present in the following documents:
  • Main text
  • pone.0084658.pdf
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Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.

Birth Defects Research. Part B, Developmental And Reproductive Toxicology
Soldano, Karen L KL; Garrett, Melanie E ME; Cope, Heidi L HL; Rusnak, J Michael JM; Ellis, Nathen J NJ; Dunlap, Kaitlyn L KL; Speer, Marcy C MC; Gregory, Simon G SG; Ashley-Koch, Allison E AE
Publication Date: 2013-10

Variant appearance in text: rs3918186
PubMed Link: 24323870
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies.

American Journal Of Medical Genetics. Part A
Browne, Marilyn L ML; Carter, Tonia C TC; Kay, Denise M DM; Kuehn, Devon D; Brody, Lawrence C LC; Romitti, Paul A PA; Liu, Aiyi A; Caggana, Michele M; Druschel, Charlotte M CM; Mills, James L JL
Publication Date: 2012-10

Variant appearance in text: rs3918186
PubMed Link: 22965740
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.

Croatian Medical Journal
Kuzmanić Samija, Radenka R; Primorac, Dragan D; Resić, Biserka B; Lozić, Bernarda B; Krzelj, Vjekoslav V; Tomasović, Maja M; Stoini, Eugenio E; Samanović, Ljubo L; Benzon, Benjamin B; Pehlić, Marina M; Boraska, Vesna V; Zemunik, Tatijana T
Publication Date: 2011-06

Variant appearance in text: rs3918186
PubMed Link: 21674837
Variant Present in the following documents:
  • Main text
  • CroatMedJ_52_0396.pdf
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Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human Molecular Genetics
Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD
Publication Date: 2009-06-15

Variant appearance in text: rs3918186
PubMed Link: 19336475
Variant Present in the following documents:
  • ddp159_1.pdf
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Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.

American Journal Of Hypertension
Vimaleswaran, Karani S KS; Franks, Paul W PW; Barroso, Inês I; Brage, Soren S; Ekelund, Ulf U; Wareham, Nicholas J NJ; Loos, Ruth J F RJ
Publication Date: 2008-03

Variant appearance in text: rs3918186
PubMed Link: 18246059
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults.

Atherosclerosis
Kullo, Iftikhar J IJ; Greene, M Todd MT; Boerwinkle, Eric E; Chu, Jian J; Turner, Stephen T ST; Kardia, Sharon L R SL
Publication Date: 2008-02

Variant appearance in text: rs3918186
PubMed Link: 17367796
Variant Present in the following documents:
  • Main text
View BVdb publication page