FOXP2 c.1647+989T>C

Variant ID: 7-114300717-T-C

NM_014491.3(FOXP2):c.1647+989T>C

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Journal Of Neurodevelopmental Disorders
Peter, Beate B; Raskind, Wendy H WH; Matsushita, Mark M; Lisowski, Mark M; Vu, Tiffany T; Berninger, Virginia W VW; Wijsman, Ellen M EM; Brkanac, Zoran Z
Publication Date: 2011-03

Variant appearance in text: rs12154391
PubMed Link: 21484596
Variant Present in the following documents:
  • Main text
  • 11689_2010_Article_9065.pdf
View BVdb publication page