NOS1AP c.177+26505A>G

Variant ID: 1-162150771-A-G

NM_014697.2(NOS1AP):c.177+26505A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

The American Journal Of Psychiatry
Wratten, Naomi S NS; Memoli, Holly H; Huang, Yungui Y; Dulencin, Anna M AM; Matteson, Paul G PG; Cornacchia, Michelle A MA; Azaro, Marco A MA; Messenger, Jaime J; Hayter, Jared E JE; Bassett, Anne S AS; Buyske, Steven S; Millonig, James H JH; Vieland, Veronica J VJ; Brzustowicz, Linda M LM
Publication Date: 2009-04

Variant appearance in text: rs6664602
PubMed Link: 19255043
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate.

Human Heredity
Kremeyer, Barbara B; García, Jenny J; Kymäläinen, Hanna H; Wratten, Naomi N; Restrepo, Gabriel G; Palacio, Carlos C; Miranda, Ana Lucía AL; López, Carlos C; Restrepo, Margarita M; Bedoya, Gabriel G; Brzustowicz, Linda M LM; Ospina-Duque, Jorge J; Arbeláez, María Patricia MP; Ruiz-Linares, Andrés A
Publication Date: 2009

Variant appearance in text: rs6664602
PubMed Link: 19077434
Variant Present in the following documents:
  • Main text
View BVdb publication page