WNT7A c.571-4155T>A

Variant ID: 3-13865075-A-T

NM_004625.3(WNT7A):c.571-4155T>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


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: rs9840696
PubMed Link: 24980784
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies.

American Journal Of Medical Genetics. Part A
Browne, Marilyn L ML; Carter, Tonia C TC; Kay, Denise M DM; Kuehn, Devon D; Brody, Lawrence C LC; Romitti, Paul A PA; Liu, Aiyi A; Caggana, Michele M; Druschel, Charlotte M CM; Mills, James L JL
Publication Date: 2012-10

Variant appearance in text: rs9840696
PubMed Link: 22965740
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.

Human Molecular Genetics
Chiquet, Brett T BT; Blanton, Susan H SH; Burt, Amber A; Ma, Deqiong D; Stal, Samuel S; Mulliken, John B JB; Hecht, Jacqueline T JT
Publication Date: 2008-07-15

Variant appearance in text: rs9840696
PubMed Link: 18413325
Variant Present in the following documents:
  • Main text
View BVdb publication page