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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.
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: 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