LRRK2 c.238-2349G>A

Variant ID: 12-40623727-G-A

NM_198578.3(LRRK2):c.238-2349G>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Mind the Gap: LRRK2 Phenotypes in the Clinic vs. in Patient Cells.

Cells
Goveas, Liesel L; Mutez, Eugénie E; Chartier-Harlin, Marie-Christine MC; Taymans, Jean-Marc JM
Publication Date: 2021-04-22

Variant appearance in text: rs11175655
PubMed Link: 33922322
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Variants Associated With Neurodegenerative Diseases Regulate Gene Expression in Immune Cell CD14+ Monocytes.

Frontiers In Genetics
Sun, Jing-Yi JY; Hou, Ya-Jun YJ; Zhang, Yan Y; Wang, Longcai L; Liu, Lidong L; Sun, Bao-Liang BL; Yuan, Hui H
Publication Date: 2018

Variant appearance in text: rs11175655
PubMed Link: 30619483
Variant Present in the following documents:
  • Main text
View BVdb publication page



Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.

Plos Genetics
Do, Chuong B CB; Tung, Joyce Y JY; Dorfman, Elizabeth E; Kiefer, Amy K AK; Drabant, Emily M EM; Francke, Uta U; Mountain, Joanna L JL; Goldman, Samuel M SM; Tanner, Caroline M CM; Langston, J William JW; Wojcicki, Anne A; Eriksson, Nicholas N
Publication Date: 2011-06

Variant appearance in text: rs11175655
PubMed Link: 21738487
Variant Present in the following documents:
  • Main text
  • pgen.1002141.pdf
View BVdb publication page



Parkinson's disease and low frequency alleles found together throughout LRRK2.

Annals Of Human Genetics
Paisán-Ruiz, Coro C; Washecka, Nicole N; Nath, Priti P; Singleton, Andrew B AB; Corder, Elizabeth H EH
Publication Date: 2009-07

Variant appearance in text: rs11175655
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
View BVdb publication page