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LRRK2 c.1941+1144T>C
Variant ID: 12-40669939-T-C
NM_198578.3(
LRRK2
):c.1941+1144T>C
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:
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: rs11564129
PubMed Link:
19489756
Variant Present in the following documents:
Main text
View BVdb publication page