LRRK2 c.237+1373G>A

Variant ID: 12-40620815-G-A

NM_198578.3(LRRK2):c.237+1373G>A

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs1491941
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Autophagy-related gene LRRK2 is likely a susceptibility gene for systemic lupus erythematosus in northern Han Chinese.

Oncotarget
Zhang, Yue-Miao YM; Zhou, Xu-Jie XJ; Cheng, Fa-Juan FJ; Qi, Yuan-Yuan YY; Hou, Ping P; Zhao, Ming-Hui MH; Zhang, Hong H
Publication Date: 2017-02-21

Variant appearance in text: rs1491941
PubMed Link: 28099919
Variant Present in the following documents:
  • Main text
  • oncotarget-08-13754.pdf
View BVdb publication page



LRRK2 gene G2019S mutation and SNPs [haplotypes] in subtypes of Parkinson's disease.

Parkinsonism & Related Disorders
Patra, Biswanath B; Parsian, Azemat J AJ; Racette, Brad A BA; Zhao, Jing Hua JH; Perlmutter, Joel S JS; Parsian, Abbas A
Publication Date: 2009-03

Variant appearance in text: rs1491941
PubMed Link: 18752982
Variant Present in the following documents:
  • Main text
View BVdb publication page



Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium.

Journal Of Medical Genetics
Paisán-Ruíz, C C; Evans, E W EW; Jain, S S; Xiromerisiou, G G; Gibbs, J R JR; Eerola, J J; Gourbali, V V; Hellström, O O; Duckworth, J J; Papadimitriou, A A; Tienari, P J PJ; Hadjigeorgiou, G M GM; Singleton, A B AB
Publication Date: 2006-02

Variant appearance in text: rs1491941
PubMed Link: 16467219
Variant Present in the following documents:
  • Main text
View BVdb publication page