IGF2BP3 c.237-17476C>T

Variant ID: 7-23475919-G-A

NM_006547.2(IGF2BP3):c.237-17476C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Polymorphic variants of IGF2BP3 and SENCR have an impact on predisposition and/or progression of Ewing sarcoma.

Frontiers In Oncology
Martinelli, Marcella M; Mancarella, Caterina C; Scapoli, Luca L; Palmieri, Annalisa A; De Sanctis, Paola P; Ferrari, Cristina C; Pasello, Michela M; Zucchini, Cinzia C; Scotlandi, Katia K
Publication Date: 2022

Variant appearance in text: rs7782764
PubMed Link: 36338681
Variant Present in the following documents:
  • Main text
  • fonc-12-968884.pdf
View BVdb publication page