RET c.74-7333G>T

Variant ID: 10-43588574-G-T

NM_020975.4(RET):c.74-7333G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease.

Genome Research
Chatterjee, Sumantra S; Karasaki, Kameko M KM; Fries, Lauren E LE; Kapoor, Ashish A; Chakravarti, Aravinda A
Publication Date: 2021-11-15

Variant appearance in text: rs7393733
PubMed Link: 34782358
Variant Present in the following documents:
  • Main text
  • 2199.pdf
View BVdb publication page