LRRK2 c.1783A>T ;(p.M595L)

Variant ID: 12-40668511-A-T

NM_198578.3(LRRK2):c.1783A>T;(p.M595L)

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:

Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populations.

Journal Of Negative Results In Biomedicine
Schlitter, Anna Melissa AM; Kurz, Martin M; Larsen, Jan P JP; Woitalla, Dirk D; Mueller, Thomas T; Epplen, Joerg T JT; Dekomien, Gabriele G
Publication Date: 2005-12-14

Variant appearance in text: LRRK2: 1783A>T
PubMed Link: 16354302
Variant Present in the following documents:
  • Main text
  • 1477-5751-4-10.pdf
View BVdb publication page