LRRK2 c.5510-268A>G

Variant ID: 12-40716694-A-G

NM_198578.3(LRRK2):c.5510-268A>G

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: rs10878372
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
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