RET c.74-713C>G

Variant ID: 10-43595194-C-G

NM_020975.4(RET):c.74-713C>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.

Plos One
Cornes, Belinda K BK; Tang, Clara S CS; Leon, Thomas Y Y TY; Hui, Kenneth J W S KJ; So, Man-Ting MT; Miao, Xiaoping X; Cherny, Stacey S SS; Sham, Pak C PC; Tam, Paul K H PK; Garcia-Barcelo, Maria-Merce MM
Publication Date: 2010-06-02

Variant appearance in text: rs3123655
PubMed Link: 20532249
Variant Present in the following documents:
  • Main text
  • pone.0010918.pdf
View BVdb publication page