LRRK2 c.5656+2392A>T

Variant ID: 12-40719500-A-T

NM_198578.3(LRRK2):c.5656+2392A>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association of NOD2 and IFNG single nucleotide polymorphisms with leprosy in the Amazon ethnic admixed population.

Plos Neglected Tropical Diseases
Leturiondo, André Luiz AL; Noronha, Ariani Batista AB; Mendonça, Carla Yael Ribeiro CYR; Ferreira, Cynthia de Oliveira CO; Alvarado-Arnez, Lucia Elena LE; Manta, Fernanda Saloum de Neves FSN; Bezerra, Ohanna Cavalcanti de Lima OCL; Carvalho, Elizeu Fagundes de EF; Moraes, Milton Ozório MO; Rodrigues, Fabíola da Costa FDC; Talhari, Carolina C
Publication Date: 2020-05

Variant appearance in text: rs7298930
PubMed Link: 32433683
Variant Present in the following documents:
  • Main text
  • pntd.0008247.pdf
View BVdb publication page



Common variants in the PARL and PINK1 genes increase the risk to leprosy in Han Chinese from South China.

Scientific Reports
Wang, Dong D; Zhang, Deng-Feng DF; Feng, Jia-Qi JQ; Li, Guo-Dong GD; Li, Xiao-An XA; Yu, Xiu-Feng XF; Long, Heng H; Li, Yu-Ye YY; Yao, Yong-Gang YG
Publication Date: 2016-11-23

Variant appearance in text: rs7298930
PubMed Link: 27876828
Variant Present in the following documents:
  • srep37086-s1.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: rs7298930
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
View BVdb publication page