NRG1 c.503-12484C>G

Variant ID: 8-32572983-C-G

NM_013964.3(NRG1):c.503-12484C>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Case Report: Primary Leptomeningeal Medulloblastoma in a Child: Clinical Case Report and Literature Review.

Frontiers In Pediatrics
Morgacheva, Daria D; Daks, Alexandra A; Smirnova, Anna A; Kim, Aleksandr A; Ryzhkova, Daria D; Mitrofanova, Lubov L; Staliarova, Alena A; Omelina, Evgeniya E; Pindyurin, Alexey A; Fedorova, Olga O; Shuvalov, Oleg O; Petukhov, Alexey A; Dinikina, Yulia Y
Publication Date: 2022

Variant appearance in text: rs2976525
PubMed Link: 35899134
Variant Present in the following documents:
  • Table_1.xlsx, sheet 1
View BVdb publication page



Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder.

Molecular Autism
Werling, Donna M DM; Lowe, Jennifer K JK; Luo, Rui R; Cantor, Rita M RM; Geschwind, Daniel H DH
Publication Date: 2014-02-17

Variant appearance in text: rs2976525
PubMed Link: 24533643
Variant Present in the following documents:
  • Main text
  • 2040-2392-5-13.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: rs2976525
PubMed Link: 22183611
Variant Present in the following documents:
  • Main text
View BVdb publication page