SNCA c.306+26381T>C

Variant ID: 4-90717016-A-G

NM_000345.3(SNCA):c.306+26381T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The alpha-synuclein gene in multiple system atrophy.

Journal Of Neurology, Neurosurgery, And Psychiatry
Ozawa, T T; Healy, D G DG; Abou-Sleiman, P M PM; Ahmadi, K R KR; Quinn, N N; Lees, A J AJ; Shaw, K K; Wullner, U U; Berciano, J J; Moller, J C JC; Kamm, C C; Burk, K K; Josephs, K A KA; Barone, P P; Tolosa, E E; Goldstein, D B DB; Wenning, G G; Geser, F F; Holton, J L JL; Gasser, T T; Revesz, T T; Wood, N W NW; ,
Publication Date: 2006-04

Variant appearance in text: rs2737028
PubMed Link: 16543523
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: rs2737028
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page