FTO c.379C>T ;(p.H127Y)

Variant ID: 16-53860031-C-T

NM_001080432.2(FTO):c.379C>T;(p.H127Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.

Breast Cancer Research : Bcr
Li, Na N; Rowley, Simone M SM; Thompson, Ella R ER; McInerny, Simone S; Devereux, Lisa L; Amarasinghe, Kaushalya C KC; Zethoven, Magnus M; Lupat, Richard R; Goode, David D; Li, Jason J; Trainer, Alison H AH; Gorringe, Kylie L KL; James, Paul A PA; Campbell, Ian G IG
Publication Date: 2018-01-09

Variant appearance in text: FTO: 379C>T
PubMed Link: 29316957
Variant Present in the following documents:
  • Main text
View BVdb publication page