GRIN2A c.1008-6805C>A

Variant ID: 16-9991762-G-T

NM_001134407.1(GRIN2A):c.1008-6805C>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic Factors Associated With Tardive Dyskinesia: From Pre-clinical Models to Clinical Studies.

Frontiers In Pharmacology
Tsermpini, Evangelia Eirini EE; Redenšek, Sara S; Dolžan, Vita V
Publication Date: 2021

Variant appearance in text: rs9921541
PubMed Link: 35140610
Variant Present in the following documents:
  • Main text
  • fphar-12-834129.pdf
View BVdb publication page



Study of Early Onset Schizophrenia: Associations of GRIN2A and GRIN2B Polymorphisms.

Life (Basel, Switzerland)
Poltavskaya, Evgeniya G EG; Fedorenko, Olga Yu OY; Kornetova, Elena G EG; Loonen, Anton J M AJM; Kornetov, Alexander N AN; Bokhan, Nikolay A NA; Ivanova, Svetlana A SA
Publication Date: 2021-09-22

Variant appearance in text: rs9921541
PubMed Link: 34685369
Variant Present in the following documents:
  • Main text
  • life-11-00997.pdf
View BVdb publication page



Antipsychotic-induced movement disorders in long-stay psychiatric patients and 45 tag SNPs in 7 candidate genes: a prospective study.

Plos One
Bakker, P Roberto PR; Al Hadithy, Asmar F Y AF; Amin, Najaf N; van Duijn, Cornelia M CM; van Os, Jim J; van Harten, Peter N PN
Publication Date: 2012

Variant appearance in text: rs9921541
PubMed Link: 23226551
Variant Present in the following documents:
  • Main text
  • pone.0050970.pdf
View BVdb publication page