FOXP2 c.1770-316G>T

Variant ID: 7-114303189-G-T

NM_014491.3(FOXP2):c.1770-316G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.

Bmc Medical Genetics
Sherva, Richard R; Sripichai, Orapan O; Abel, Kenneth K; Ma, Qianli Q; Whitacre, Johanna J; Angkachatchai, Vach V; Makarasara, Wattanan W; Winichagoon, Pranee P; Svasti, Saovaros S; Fucharoen, Suthat S; Braun, Andreas A; Farrer, Lindsay A LA
Publication Date: 2010-03-30

Variant appearance in text: rs1563408
PubMed Link: 20353593
Variant Present in the following documents:
  • Main text
  • 1471-2350-11-51.pdf
View BVdb publication page