LRRK2 c.6382-566A>C

Variant ID: 12-40744775-A-C

NM_198578.3(LRRK2):c.6382-566A>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses in Leprosy.

Plos Neglected Tropical Diseases
Fava, Vinicius M VM; Manry, Jérémy J; Cobat, Aurélie A; Orlova, Marianna M; Van Thuc, Nguyen N; Ba, Nguyen Ngoc NN; Thai, Vu Hong VH; Abel, Laurent L; Alcaïs, Alexandre A; Schurr, Erwin E; ,
Publication Date: 2016-02

Variant appearance in text: rs7303525
PubMed Link: 26844546
Variant Present in the following documents:
  • Main text
  • pntd.0004412.pdf
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: rs7303525
PubMed Link: 16467219
Variant Present in the following documents:
  • Main text
View BVdb publication page