LRRK2 c.572-971T>G

Variant ID: 12-40633314-T-G

NM_198578.3(LRRK2):c.572-971T>G

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: rs10878249
PubMed Link: 26844546
Variant Present in the following documents:
  • Main text
  • pntd.0004412.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: rs10878249
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
View BVdb publication page