LRRK2 c.1941+1144T>C

Variant ID: 12-40669939-T-C

NM_198578.3(LRRK2):c.1941+1144T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs11564129
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
View BVdb publication page