NRG1 c.502+32746C>T

Variant ID: 8-32507149-C-T

NM_013964.3(NRG1):c.502+32746C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Meta-analysis reveals associations between genetic variation in the 5' and 3' regions of Neuregulin-1 and schizophrenia.

Translational Psychiatry
Mostaid, M S MS; Mancuso, S G SG; Liu, C C; Sundram, S S; Pantelis, C C; Everall, I P IP; Bousman, C A CA
Publication Date: 2017-01-17

Variant appearance in text: rs2466058
PubMed Link: 28094814
Variant Present in the following documents:
  • Main text
  • tp2016279a.pdf
View BVdb publication page



Genetic associations between neuregulin-1 SNPs and neurocognitive function in multigenerational, multiplex schizophrenia families.

Psychiatric Genetics
Yokley, Jessica L JL; Prasad, Konasale M KM; Chowdari, Kodavali V KV; Talkowski, Michael E ME; Wood, Joel J; Gur, Ruben C RC; Gur, Raquel E RE; Almasy, Laura L; Nimgaonkar, Vishwajit L VL; Pogue-Geile, Michael F MF
Publication Date: 2012-04

Variant appearance in text: rs2466058
PubMed Link: 22183611
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of a promoter polymorphism in the SMDF neuregulin 1 isoform in Schizophrenia.

Neuropsychobiology
Pedrosa, Erika E; Nolan, Karen A KA; Stefanescu, Radu R; Herskovits, Pnina P; Hershcovitz, Pnina P; Novak, Tomas T; Zukov, Ilja I; Stopkova, Pavla P; Lachman, Herbert M HM
Publication Date: 2009

Variant appearance in text: rs2466058
PubMed Link: 19521112
Variant Present in the following documents:
  • Main text
View BVdb publication page