WRN c.2088+4222A>C

Variant ID: 8-30962693-A-C

NM_000553.4(WRN):c.2088+4222A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family.

Frontiers In Oncology
Norouzi, Mahnaz M; Shafiei, Mohammad M; Abdollahi, Zeinab Z; Miar, Paniz P; Galehdari, Hamid H; Emami, Mohammad Hasan MH; Zeinalian, Mehrdad M; Tabatabaiefar, Mohammad Amin MA
Publication Date: 2021

Variant appearance in text: rs9649886
PubMed Link: 34164337
Variant Present in the following documents:
  • Main text
  • fonc-11-648649.pdf
View BVdb publication page