LRRK2 c.4946A>C ;(p.Y1649S)

Variant ID: 12-40713908-A-C

NM_198578.3(LRRK2):c.4946A>C;(p.Y1649S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.

Frontiers In Genetics
Illés, Anett A; Csabán, Dóra D; Grosz, Zoltán Z; Balicza, Péter P; Gézsi, András A; Molnár, Viktor V; Bencsik, Renáta R; Gál, Anikó A; Klivényi, Péter P; Molnar, Maria Judit MJ
Publication Date: 2019

Variant appearance in text: LRRK2: 4946A>C; Y1649S
PubMed Link: 31737044
Variant Present in the following documents:
  • Main text
  • fgene-10-01061.pdf
View BVdb publication page