LRRK2 c.1656+3700A>T

Variant ID: 12-40661403-A-T

NM_198578.3(LRRK2):c.1656+3700A>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain.

Neurogenetics
Mata, Ignacio F IF; Hutter, Carolyn M CM; González-Fernández, María C MC; de Pancorbo, Marian M MM; Lezcano, Elena E; Huerta, Cecilia C; Blazquez, Marta M; Ribacoba, Renee R; Guisasola, Luis M LM; Salvador, Carlos C; Gómez-Esteban, Juan C JC; Zarranz, Juan J JJ; Infante, Jon J; Jankovic, Joseph J; Deng, Hao H; Edwards, Karen L KL; Alvarez, Victoria V; Zabetian, Cyrus P CP
Publication Date: 2009-10

Variant appearance in text: rs4768224
PubMed Link: 19308469
Variant Present in the following documents:
  • Main text
View BVdb publication page



Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium.

Journal Of Medical Genetics
Paisán-Ruíz, C C; Evans, E W EW; Jain, S S; Xiromerisiou, G G; Gibbs, J R JR; Eerola, J J; Gourbali, V V; Hellström, O O; Duckworth, J J; Papadimitriou, A A; Tienari, P J PJ; Hadjigeorgiou, G M GM; Singleton, A B AB
Publication Date: 2006-02

Variant appearance in text: rs4768224
PubMed Link: 16467219
Variant Present in the following documents:
  • Main text
View BVdb publication page