LRRK2 c.238-995G>A

Variant ID: 12-40625081-G-A

NM_198578.3(LRRK2):c.238-995G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Mind the Gap: LRRK2 Phenotypes in the Clinic vs. in Patient Cells.

Cells
Goveas, Liesel L; Mutez, Eugénie E; Chartier-Harlin, Marie-Christine MC; Taymans, Jean-Marc JM
Publication Date: 2021-04-22

Variant appearance in text: rs74324737
PubMed Link: 33922322
Variant Present in the following documents:
  • Main text
View BVdb publication page



Enrichment of risk SNPs in regulatory regions implicate diverse tissues in Parkinson's disease etiology.

Scientific Reports
Coetzee, Simon G SG; Pierce, Steven S; Brundin, Patrik P; Brundin, Lena L; Hazelett, Dennis J DJ; Coetzee, Gerhard A GA
Publication Date: 2016-07-27

Variant appearance in text: rs74324737
PubMed Link: 27461410
Variant Present in the following documents:
  • Main text
  • srep30509.pdf
View BVdb publication page