SNCA c.306+9728T>C

Variant ID: 4-90733669-A-G

NM_000345.3(SNCA):c.306+9728T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.

Plos One
Al-Chalabi, Ammar A; Dürr, Alexandra A; Wood, Nicholas W NW; Parkinson, Michael H MH; Camuzat, Agnes A; Hulot, Jean-Sébastien JS; Morrison, Karen E KE; Renton, Alan A; Sussmuth, Sigurd D SD; Landwehrmeyer, Bernhard G BG; Ludolph, Albert A; Agid, Yves Y; Brice, Alexis A; Leigh, P Nigel PN; Bensimon, Gilbert G; ,
Publication Date: 2009-09-22

Variant appearance in text: rs2619369
PubMed Link: 19771175
Variant Present in the following documents:
  • Main text
  • pone.0007114.pdf
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: rs2619369
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page