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LRRK2 c.4317+117C>A
Variant ID: 12-40703152-C-A
NM_198578.3(
LRRK2
):c.4317+117C>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:
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
Parkinsonism & Related Disorders
Ross, Owen A OA; Spanaki, Cleanthe C; Griffith, Alida A; Lin, Chin-Hsien CH; Kachergus, Jennifer J; Haugarvoll, Kristoffer K; Latsoudis, Helen H; Plaitakis, Andreas A; Ferreira, Joaquim J JJ; Sampaio, Cristina C; Bonifati, Vincenzo V; Wu, Ruey-Meei RM; Zabetian, Cyrus P CP; Farrer, Matthew J MJ
Publication Date: 2009-07
Variant appearance in text: rs11175966
PubMed Link:
18952485
Variant Present in the following documents:
Main text
View BVdb publication page