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PLPP3 c.139+18787G>A
Variant ID: 1-57025764-C-T
NM_003713.4(
PLPP3
):c.139+18787G>A
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:
Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
American Journal Of Human Genetics
Oliveira, Sofia A SA; Li, Yi-Ju YJ; Noureddine, Maher A MA; Zuchner, Stephan S; Qin, Xuejun X; Pericak-Vance, Margaret A MA; Vance, Jeffery M JM
Publication Date: 2005-08
Variant appearance in text: rs1777284
PubMed Link:
15986317
Variant Present in the following documents:
Main text
View BVdb publication page