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LRRK2 c.4537-496C>T
Variant ID: 12-40707278-C-T
NM_198578.3(
LRRK2
):c.4537-496C>T
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:
Genetic variations in cancer-related significantly mutated genes and lung cancer susceptibility.
Annals Of Oncology : Official Journal Of The European Society For Medical Oncology
Zhang, Y Y; Zhang, L L; Li, R R; Chang, D W DW; Ye, Y Y; Minna, J D JD; Roth, J A JA; Han, B B; Wu, X X
Publication Date: 2017-07-01
Variant appearance in text: rs11175985
PubMed Link:
28383694
Variant Present in the following documents:
Main text
View BVdb publication page
Parkinson's disease and low frequency alleles found together throughout LRRK2.
Annals Of Human Genetics
Paisán-Ruiz, Coro C; Washecka, Nicole N; Nath, Priti P; Singleton, Andrew B AB; Corder, Elizabeth H EH
Publication Date: 2009-07
Variant appearance in text: rs11175985
PubMed Link:
19489756
Variant Present in the following documents:
Main text
View BVdb publication page