LRRK2 c.2242-1477G>T

Variant ID: 12-40676200-G-T

NM_198578.3(LRRK2):c.2242-1477G>T

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Uncovering the complex genetics of human character.

Molecular Psychiatry
Zwir, Igor I; Arnedo, Javier J; Del-Val, Coral C; Pulkki-Råback, Laura L; Konte, Bettina B; Yang, Sarah S SS; Romero-Zaliz, Rocio R; Hintsanen, Mirka M; Cloninger, Kevin M KM; Garcia, Danilo D; Svrakic, Dragan M DM; Rozsa, Sandor S; Martinez, Maribel M; Lyytikäinen, Leo-Pekka LP; Giegling, Ina I; Kähönen, Mika M; Hernandez-Cuervo, Helena H; Seppälä, Ilkka I; Raitoharju, Emma E; de Erausquin, Gabriel A GA; Raitakari, Olli O; Rujescu, Dan D; Postolache, Teodor T TT; Sung, Joohon J; Keltikangas-Järvinen, Liisa L; Lehtimäki, Terho T; Cloninger, C Robert CR
Publication Date: 2020-10

Variant appearance in text: LRRK2: 2242-1477G>T; rs11175847
PubMed Link: 30283034
Variant Present in the following documents:
  • 41380_2018_263_MOESM14_ESM.xlsx, sheet 1
View BVdb publication page



Uncovering the complex genetics of human temperament.

Molecular Psychiatry
Zwir, Igor I; Arnedo, Javier J; Del-Val, Coral C; Pulkki-Råback, Laura L; Konte, Bettina B; Yang, Sarah S SS; Romero-Zaliz, Rocio R; Hintsanen, Mirka M; Cloninger, Kevin M KM; Garcia, Danilo D; Svrakic, Dragan M DM; Rozsa, Sandor S; Martinez, Maribel M; Lyytikäinen, Leo-Pekka LP; Giegling, Ina I; Kähönen, Mika M; Hernandez-Cuervo, Helena H; Seppälä, Ilkka I; Raitoharju, Emma E; de Erausquin, Gabriel A GA; Raitakari, Olli O; Rujescu, Dan D; Postolache, Teodor T TT; Sung, Joohon J; Keltikangas-Järvinen, Liisa L; Lehtimäki, Terho T; Cloninger, C Robert CR
Publication Date: 2020-10

Variant appearance in text: LRRK2: 2242-1477G>T; rs11175847
PubMed Link: 30279457
Variant Present in the following documents:
  • 41380_2018_264_MOESM15_ESM.xlsx, sheet 1
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: rs11175847
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: rs11175847
PubMed Link: 19489756
Variant Present in the following documents:
  • Main text
View BVdb publication page