KIAA0319 c.-106+4359G>A

Variant ID: 6-24641605-C-T

NM_014809.4(KIAA0319):c.-106+4359G>A

This variant was identified in 4 publications

View GRCh38 version.




Publications:


A genome-wide association study identifies a new variant associated with word reading fluency in Chinese children.

Genes, Brain, And Behavior
Wang, Zhengjun Z; Zhao, Shunan S; Zhang, Liming L; Yang, Qing Q; Cheng, Chen C; Ding, Ning N; Zhu, Zijian Z; Shu, Hua H; Liu, Chunyu C; Zhao, Jingjing J
Publication Date: 2022-12-13

Variant appearance in text: rs16889556
PubMed Link: 36514817
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identifying interactive biological pathways associated with reading disability.

Brain And Behavior
Lancaster, Hope Sparks HS; Liu, Xiaonan X; Dinu, Valentin V; Li, Jing J
Publication Date: 2020-08

Variant appearance in text: rs16889556
PubMed Link: 32596987
Variant Present in the following documents:
  • Main text
  • BRB3-10-e01735.pdf
View BVdb publication page



KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.

Journal Of Human Genetics
Zhao, Hua H; Chen, Yun Y; Zhang, Bao-Ping BP; Zuo, Peng-Xiang PX
Publication Date: 2016-08

Variant appearance in text: rs16889556
PubMed Link: 27098879
Variant Present in the following documents:
  • Main text
  • jhg201640a.pdf
View BVdb publication page



Genome-wide association study of shared components of reading disability and language impairment.

Genes, Brain, And Behavior
Eicher, J D JD; Powers, N R NR; Miller, L L LL; Akshoomoff, N N; Amaral, D G DG; Bloss, C S CS; Libiger, O O; Schork, N J NJ; Darst, B F BF; Casey, B J BJ; Chang, L L; Ernst, T T; Frazier, J J; Kaufmann, W E WE; Keating, B B; Kenet, T T; Kennedy, D D; Mostofsky, S S; Murray, S S SS; Sowell, E R ER; Bartsch, H H; Kuperman, J M JM; Brown, T T TT; Hagler, D J DJ; Dale, A M AM; Jernigan, T L TL; St Pourcain, B B; Davey Smith, G G; Ring, S M SM; Gruen, J R JR; ,
Publication Date: 2013-11

Variant appearance in text: rs16889556
PubMed Link: 24024963
Variant Present in the following documents:
  • Main text
  • gbb0012-0792.pdf
View BVdb publication page