LRRK2 c.238-1766A>G

Variant ID: 12-40624310-A-G

NM_198578.3(LRRK2):c.238-1766A>G

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: rs11175658
PubMed Link: 33922322
Variant Present in the following documents:
  • Main text
View BVdb publication page