WNT7A c.298+8373A>C

Variant ID: 3-13908071-T-G

NM_004625.3(WNT7A):c.298+8373A>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic Predisposition for Renal Dysfunction and Incidence of CKD in the Malmö Diet and Cancer Study.

Kidney International Reports
Schulz, Christina-Alexandra CA; Engström, Gunnar G; Christensson, Anders A; Nilsson, Peter M PM; Melander, Olle O; Orho-Melander, Marju M
Publication Date: 2019-08

Variant appearance in text: rs9864031
PubMed Link: 31440704
Variant Present in the following documents:
  • Main text
  • main.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: rs9864031
PubMed Link: 24980784
Variant Present in the following documents:
  • Main text
View BVdb publication page