WNT2 c.854-1540C>T

Variant ID: 7-116919978-G-A

NM_003391.2(WNT2):c.854-1540C>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


A translational exploration of the effects of WNT2 variants on altered cortical structures in autism spectrum disorder.

Journal Of Psychiatry & Neuroscience : Jpn
Chien, Yi-Ling YL; Chen, Yu-Chieh YC; Chiu, Yen-Nan YN; Tsai, Wen-Che WC; Gau, Susan Shur-Fen SS
Publication Date: 2021

Variant appearance in text: rs2896218
PubMed Link: 34862305
Variant Present in the following documents:
  • Main text
  • 46-6-E647.pdf
View BVdb publication page



A systematic review of common genetic variation and biological pathways in autism spectrum disorder.

Bmc Neuroscience
Rodriguez-Gomez, Diego Alejandro DA; Garcia-Guaqueta, Danna Paola DP; Charry-Sánchez, Jesús David JD; Sarquis-Buitrago, Elias E; Blanco, Mariana M; Velez-van-Meerbeke, Alberto A; Talero-Gutiérrez, Claudia C
Publication Date: 2021-10-09

Variant appearance in text: rs2896218
PubMed Link: 34627165
Variant Present in the following documents:
  • 12868_2021_662_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



MGST2 and WNT2 are candidate genes for comitant strabismus susceptibility in Japanese patients.

Peerj
Zhang, Jingjing J; Matsuo, Toshihiko T
Publication Date: 2017

Variant appearance in text: rs2896218
PubMed Link: 29062608
Variant Present in the following documents:
  • Main text
  • peerj-05-3935.pdf
View BVdb publication page



Genetic polymorphisms of Wnt/β-catenin pathway genes are associated with the efficacy and toxicities of radiotherapy in patients with nasopharyngeal carcinoma.

Oncotarget
Yu, Jingjing J; Huang, Yuling Y; Liu, Lijuan L; Wang, Jing J; Yin, Jiye J; Huang, Lihua L; Chen, Shaojun S; Li, Jingao J; Yuan, Hong H; Yang, Guoping G; Liu, Wenyu W; Wang, Hai H; Pei, Qi Q; Guo, Chengxian C
Publication Date: 2016-12-13

Variant appearance in text: rs2896218
PubMed Link: 27769064
Variant Present in the following documents:
  • Main text
View BVdb publication page



Formation of functional areas in the cerebral cortex is disrupted in a mouse model of autism spectrum disorder.

Neural Development
Fenlon, Laura R LR; Liu, Sha S; Gobius, Ilan I; Kurniawan, Nyoman D ND; Murphy, Skyle S; Moldrich, Randal X RX; Richards, Linda J LJ
Publication Date: 2015-04-03

Variant appearance in text: rs2896218
PubMed Link: 25879444
Variant Present in the following documents:
  • Main text
  • 13064_2015_Article_33.pdf
View BVdb publication page



Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.

The Pharmacogenomics Journal
Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X
Publication Date: 2014-12

Variant appearance in text: rs2896218
PubMed Link: 24980784
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multifaceted genomic risk for brain function in schizophrenia.

Neuroimage
Chen, Jiayu J; Calhoun, Vince D VD; Pearlson, Godfrey D GD; Ehrlich, Stefan S; Turner, Jessica A JA; Ho, Beng-Choon BC; Wassink, Thomas H TH; Michael, Andrew M AM; Liu, Jingyu J
Publication Date: 2012-07-16

Variant appearance in text: rs2896218
PubMed Link: 22440650
Variant Present in the following documents:
  • Main text
View BVdb publication page