Bibliome.ai browser hg19
Search
About
Stats
FAQ
LRRK2 c.838+2078A>T
Variant ID: 12-40639561-A-T
NM_198578.3(
LRRK2
):c.838+2078A>T
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:
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: rs2404580
PubMed Link:
26844546
Variant Present in the following documents:
Main text
pntd.0004412.pdf
View BVdb publication page