RTN4R c.22+9513A>T

Variant ID: 22-20246081-T-A

NM_023004.5(RTN4R):c.22+9513A>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The rs696880 Polymorphism in the Nogo-A Receptor Gene (RTN4R) Is Associated With Susceptibility to Sporadic Amyotrophic Lateral Sclerosis in the Chinese Population.

Frontiers In Aging Neuroscience
Xu, Lianping L; Li, Jiao J; Tian, Danyang D; Chen, Lu L; Tang, Lu L; Fan, Dongsheng D
Publication Date: 2018

Variant appearance in text: rs701421
PubMed Link: 29706887
Variant Present in the following documents:
  • Main text
  • fnagi-10-00108.pdf
View BVdb publication page



Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.

The Journal Of Neuroscience : The Official Journal Of The Society For Neuroscience
Budel, Stéphane S; Padukkavidana, Thihan T; Liu, Betty P BP; Feng, Zeny Z; Hu, Fenghua F; Johnson, Sam S; Lauren, Juha J; Park, James H JH; McGee, Aaron W AW; Liao, Ji J; Stillman, Althea A; Kim, Ji-Eun JE; Yang, Bao-Zhu BZ; Sodi, Stefano S; Gelernter, Joel J; Zhao, Hongyu H; Hisama, Fuki F; Arnsten, Amy F T AF; Strittmatter, Stephen M SM
Publication Date: 2008-12-03

Variant appearance in text: rs701421
PubMed Link: 19052207
Variant Present in the following documents:
  • Main text
View BVdb publication page