LRRK2 c.7029-732C>T

Variant ID: 12-40756472-C-T

NM_198578.3(LRRK2):c.7029-732C>T

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs4768236
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy.

Plos Genetics
Fava, Vinicius M VM; Manry, Jeremy J; Cobat, Aurélie A; Orlova, Marianna M; Van Thuc, Nguyen N; Moraes, Milton O MO; Sales-Marques, Carolinne C; Stefani, Mariane M A MM; Latini, Ana Carla P AC; Belone, Andrea F AF; Thai, Vu Hong VH; Abel, Laurent L; Alcaïs, Alexandre A; Schurr, Erwin E
Publication Date: 2017-02

Variant appearance in text: rs4768236
PubMed Link: 28222097
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs4768236
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: rs4768236
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
View BVdb publication page