NOS1AP c.940-3786G>A

Variant ID: 1-162331408-G-A

NM_014697.2(NOS1AP):c.940-3786G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A primerless molecular diagnostic: phosphorothioated-terminal hairpin formation and self-priming extension (PS-THSP).

Analytical And Bioanalytical Chemistry
Jung, Cheulhee C; Ellington, Andrew D AD
Publication Date: 2016-12

Variant appearance in text: rs12122048
PubMed Link: 27032410
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: rs12122048
PubMed Link: 19077434
Variant Present in the following documents:
  • Main text
View BVdb publication page



Improvements to bead-based oligonucleotide ligation SNP genotyping assays.

Biotechniques
Bruse, Shannon S; Moreau, Michael M; Azaro, Marco M; Zimmerman, Ray R; Brzustowicz, Linda L
Publication Date: 2008-11

Variant appearance in text: rs12122048
PubMed Link: 19007340
Variant Present in the following documents:
  • Main text
View BVdb publication page