NOS1AP c.106-398A>G

Variant ID: 1-162123797-A-G

NM_014697.2(NOS1AP):c.106-398A>G

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Association of nitric oxide synthase 1 adaptor protein gene polymorphisms with schizophrenia in a Chinese Han population.

Indian Journal Of Psychiatry
Yang, Xueping X; Zhou, Jing J; Yuan, Zhen Z; Lin, Ailu A; Li, Xin X; Cong, Zhengtu Z; He, Ru R; Zhu, Gang G
Publication Date: 2022

Variant appearance in text: rs4656355
PubMed Link: 35494330
Variant Present in the following documents:
  • Main text
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: rs4656355
PubMed Link: 32111088
Variant Present in the following documents:
  • Main text
  • ijms-21-01604.pdf
View BVdb publication page



Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.

Human Molecular Genetics
Kocarnik, Jonathan M JM; Richard, Melissa M; Graff, Misa M; Haessler, Jeffrey J; Bien, Stephanie S; Carlson, Chris C; Carty, Cara L CL; Reiner, Alexander P AP; Avery, Christy L CL; Ballantyne, Christie M CM; LaCroix, Andrea Z AZ; Assimes, Themistocles L TL; Barbalic, Maja M; Pankratz, Nathan N; Tang, Weihong W; Tao, Ran R; Chen, Dongquan D; Talavera, Gregory A GA; Daviglus, Martha L ML; Chirinos-Medina, Diana A DA; Pereira, Rocio R; Nishimura, Katie K; Bužková, Petra P; Best, Lyle G LG; Ambite, José Luis JL; Cheng, Iona I; Crawford, Dana C DC; Hindorff, Lucia A LA; Fornage, Myriam M; Heiss, Gerardo G; North, Kari E KE; Haiman, Christopher A CA; Peters, Ulrike U; Le Marchand, Loic L; Kooperberg, Charles C
Publication Date: 2018-08-15

Variant appearance in text: rs4656355
PubMed Link: 29878111
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease.

Circulation. Cardiovascular Genetics
Westaway, Shawn K SK; Reinier, Kyndaron K; Huertas-Vazquez, Adriana A; Evanado, Audrey A; Teodorescu, Carmen C; Navarro, Jo J; Sinner, Moritz F MF; Gunson, Karen K; Jui, Jonathan J; Spooner, Peter P; Kaab, Stefan S; Chugh, Sumeet S SS
Publication Date: 2011-08-01

Variant appearance in text: rs4656355
PubMed Link: 21685173
Variant Present in the following documents:
  • Main text
View BVdb publication page