NCAN c.3115G>T ;(p.A1039S)

Variant ID: 19-19344693-G-T

NM_004386.2(NCAN):c.3115G>T;(p.A1039S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of NCAN as a candidate gene for developmental dyslexia.

Scientific Reports
Einarsdottir, Elisabet E; Peyrard-Janvid, Myriam M; Darki, Fahimeh F; Tuulari, Jetro J JJ; Merisaari, Harri H; Karlsson, Linnea L; Scheinin, Noora M NM; Saunavaara, Jani J; Parkkola, Riitta R; Kantojärvi, Katri K; Ämmälä, Antti-Jussi AJ; Yiu-Lin Yu, Nancy N; Matsson, Hans H; Nopola-Hemmi, Jaana J; Karlsson, Hasse H; Paunio, Tiina T; Klingberg, Torkel T; Leinonen, Eira E; Kere, Juha J
Publication Date: 2017-08-24

Variant appearance in text: rs146011974
PubMed Link: 28839234
Variant Present in the following documents:
  • 41598_2017_10175_MOESM1_ESM.pdf
View BVdb publication page