WNT2 c.588+6954G>T

Variant ID: 7-116948171-C-A

NM_003391.2(WNT2):c.588+6954G>T

This variant was identified in 2 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: rs2285545
PubMed Link: 34862305
Variant Present in the following documents:
  • Main text
  • 46-6-E647.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: rs2285545
PubMed Link: 24980784
Variant Present in the following documents:
  • Main text
View BVdb publication page