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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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