NOS1AP c.106-32911C>T

Variant ID: 1-162091284-C-T

NM_014697.2(NOS1AP):c.106-32911C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Robust Reference Powered Association Test of Genome-Wide Association Studies.

Frontiers In Genetics
Wang, Yi Y; Li, Yi Y; Hao, Meng M; Liu, Xiaoyu X; Zhang, Menghan M; Wang, Jiucun J; Xiong, Momiao M; Shugart, Yin Yao YY; Jin, Li L
Publication Date: 2019

Variant appearance in text: rs12140791
PubMed Link: 31024629
Variant Present in the following documents:
  • Main text
  • fgene-10-00319.pdf
View BVdb publication page



Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder.

Translational Psychiatry
Lee, P H PH; Perlis, R H RH; Jung, J-Y JY; Byrne, E M EM; Rueckert, E E; Siburian, R R; Haddad, S S; Mayerfeld, C E CE; Heath, A C AC; Pergadia, M L ML; Madden, P A F PA; Boomsma, D I DI; Penninx, B W BW; Sklar, P P; Martin, N G NG; Wray, N R NR; Purcell, S M SM; Smoller, J W JW
Publication Date: 2012-11-13

Variant appearance in text: rs12140791
PubMed Link: 23149448
Variant Present in the following documents:
  • tp201295x1.pdf
View BVdb publication page



Strong synaptic transmission impact by copy number variations in schizophrenia.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Glessner, Joseph T JT; Reilly, Muredach P MP; Kim, Cecilia E CE; Takahashi, Nagahide N; Albano, Anthony A; Hou, Cuiping C; Bradfield, Jonathan P JP; Zhang, Haitao H; Sleiman, Patrick M A PM; Flory, James H JH; Imielinski, Marcin M; Frackelton, Edward C EC; Chiavacci, Rosetta R; Thomas, Kelly A KA; Garris, Maria M; Otieno, Frederick G FG; Davidson, Michael M; Weiser, Mark M; Reichenberg, Abraham A; Davis, Kenneth L KL; Friedman, Joseph I JI; Cappola, Thomas P TP; Margulies, Kenneth B KB; Rader, Daniel J DJ; Grant, Struan F A SF; Buxbaum, Joseph D JD; Gur, Raquel E RE; Hakonarson, Hakon H
Publication Date: 2010-06-08

Variant appearance in text: rs12140791
PubMed Link: 20489179
Variant Present in the following documents:
  • Main text
View BVdb publication page