SNCA c.307-37499C>T

Variant ID: 4-90687927-G-A

NM_000345.3(SNCA):c.307-37499C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population.

Parkinsonism & Related Disorders
Trotta, Luca L; Guella, Ilaria I; Soldà, Giulia G; Sironi, Francesca F; Tesei, Silvana S; Canesi, Margherita M; Pezzoli, Gianni G; Goldwurm, Stefano S; Duga, Stefano S; Asselta, Rosanna R
Publication Date: 2012-03

Variant appearance in text: rs356192
PubMed Link: 22104010
Variant Present in the following documents:
  • Main text
View BVdb publication page



Linkage disequilibrium patterns and tagSNP transferability among European populations.

American Journal Of Human Genetics
Mueller, Jakob C JC; Lõhmussaar, Elin E; Mägi, Reedik R; Remm, Maido M; Bettecken, Thomas T; Lichtner, Peter P; Biskup, Saskia S; Illig, Thomas T; Pfeufer, Arne A; Luedemann, Jan J; Schreiber, Stefan S; Pramstaller, Peter P; Pichler, Irene I; Romeo, Giovanni G; Gaddi, Anthony A; Testa, Alessandra A; Wichmann, Heinz-Erich HE; Metspalu, Andres A; Meitinger, Thomas T
Publication Date: 2005-03

Variant appearance in text: rs356192
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page