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LRRK2 c.572-971T>G
Variant ID: 12-40633314-T-G
NM_198578.3(
LRRK2
):c.572-971T>G
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:
A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses in Leprosy.
Plos Neglected Tropical Diseases
Fava, Vinicius M VM; Manry, Jérémy J; Cobat, Aurélie A; Orlova, Marianna M; Van Thuc, Nguyen N; Ba, Nguyen Ngoc NN; Thai, Vu Hong VH; Abel, Laurent L; Alcaïs, Alexandre A; Schurr, Erwin E; ,
Publication Date: 2016-02
Variant appearance in text: rs10878249
PubMed Link:
26844546
Variant Present in the following documents:
Main text
pntd.0004412.pdf
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: rs10878249
PubMed Link:
19489756
Variant Present in the following documents:
Main text
View BVdb publication page