NOS2 c.204A>G ;(p.P68=)

Variant ID: 17-26115949-T-C

NM_000625.4(NOS2):c.204A>G;(p.P68=)

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Are Genetic Modifiers the Answer to Different Responses to Hydroxyurea Treatment?-A Pharmacogenetic Study in Sickle Cell Anemia Angolan Children.

International Journal Of Molecular Sciences
Ginete, Catarina C; Delgadinho, Mariana M; Santos, Brígida B; Pinto, Vera V; Silva, Carina C; Miranda, Armandina A; Brito, Miguel M
Publication Date: 2023-05-15

Variant appearance in text: rs16966563
PubMed Link: 37240136
Variant Present in the following documents:
  • Main text
  • ijms-24-08792.pdf
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: NOS2: P68P
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
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: rs16966563
PubMed Link: 32111088
Variant Present in the following documents:
  • Main text
  • ijms-21-01604.pdf
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: NOS2: P68P; rs16966563
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



NOS2 variants reveal a dual genetic control of nitric oxide levels, susceptibility to Plasmodium infection, and cerebral malaria.

Infection And Immunity
Trovoada, Maria de Jesus Mde J; Martins, Madalena M; Ben Mansour, Riadh R; Sambo, Maria do Rosário Mdo R; Fernandes, Ana B AB; Antunes Gonçalves, Lígia L; Borja, Artur A; Moya, Roni R; Almeida, Paulo P; Costa, João J; Marques, Isabel I; Macedo, M Paula MP; Coutinho, António A; Narum, David L DL; Penha-Gonçalves, Carlos C
Publication Date: 2014-03

Variant appearance in text: rs16966563
PubMed Link: 24379293
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of single nucleotide polymorphisms in the NOS2A gene and interaction with smoking in age-related macular degeneration.

Annals Of Human Genetics
Ayala-Haedo, Juan A JA; Gallins, Paul J PJ; Whitehead, Patrice L PL; Schwartz, Stephen G SG; Kovach, Jaclyn L JL; Postel, Eric A EA; Agarwal, Anita A; Wang, Gaofeng G; Haines, Jonathan L JL; Pericak-Vance, Margaret A MA; Scott, William K WK
Publication Date: 2010-05

Variant appearance in text: NOS2A: P68P; rs16966563
PubMed Link: 20374233
Variant Present in the following documents:
  • Main text
View BVdb publication page



Nitric oxide synthase 2A (NOS2A) polymorphisms are not associated with invasive pneumococcal disease.

Bmc Medical Genetics
Payton, Antony A; Payne, Debbie D; Mankhambo, Limangeni A LA; Banda, Daniel L DL; Hart, C Anthony CA; Ollier, William Er WE; Carrol, Enitan D ED
Publication Date: 2009-03-23

Variant appearance in text: NOS2A: Pro68Pro; rs16966563
PubMed Link: 19309520
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-28.pdf
View BVdb publication page



Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.

Neurogenetics
Hancock, Dana B DB; Martin, Eden R ER; Vance, Jeffery M JM; Scott, William K WK
Publication Date: 2008-10

Variant appearance in text: rs16966563
PubMed Link: 18663495
Variant Present in the following documents:
  • Main text
View BVdb publication page