LRRK2 c.4537-496C>T

Variant ID: 12-40707278-C-T

NM_198578.3(LRRK2):c.4537-496C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic variations in cancer-related significantly mutated genes and lung cancer susceptibility.

Annals Of Oncology : Official Journal Of The European Society For Medical Oncology
Zhang, Y Y; Zhang, L L; Li, R R; Chang, D W DW; Ye, Y Y; Minna, J D JD; Roth, J A JA; Han, B B; Wu, X X
Publication Date: 2017-07-01

Variant appearance in text: rs11175985
PubMed Link: 28383694
Variant Present in the following documents:
  • Main text
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: rs11175985
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
View BVdb publication page