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LRRK2 c.5687C>G ;(p.A1896G)
Variant ID: 12-40722192-C-G
NM_198578.3(
LRRK2
):c.5687C>G;(p.A1896G)
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:
Parkinson's Disease and Fabry Disease: Clinical, Biochemical and Neuroimaging Analysis of Three Pedigrees.
Journal Of Parkinson'S Disease
Gago, Miguel Fernandes MF; Azevedo, Olga O; GuimarĂ£es, Andreia A; Teresa Vide, Ana A; Lamas, Nuno J NJ; Oliveira, Tiago Gil TG; Gaspar, Paulo P; Bicho, Estela E; Miltenberger-Miltenyi, Gabriel G; Ferreira, Joaquim J; Sousa, Nuno N
Publication Date: 2020
Variant appearance in text: LRRK2: 5687C>G; Ala1896Gly
PubMed Link:
31594250
Variant Present in the following documents:
Main text
jpd-10-jpd191704.pdf
View BVdb publication page