SNCA c.306+21837T>C

Variant ID: 4-90721560-A-G

NM_000345.3(SNCA):c.306+21837T>C

This variant was identified in 5 publications

View GRCh38 version.




Publications:


The cis-Regulatory Element of SNCA Intron 4 Modulates Susceptibility to Parkinson's Disease in Han Chinese.

Frontiers In Genetics
Zhu, Shi-Guo SG; Lu, Hui H; Mao, Miao M; Li, Zhao-Feng ZF; Cui, Lei L; Ovlyakulov, Begench B; Zhang, Xiong X; Zhu, Jian-Hong JH
Publication Date: 2020

Variant appearance in text: rs2737024
PubMed Link: 33193729
Variant Present in the following documents:
  • Main text
  • fgene-11-590365.pdf
View BVdb publication page



Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies.

Annals Of Neurology
Krohn, Lynne L; Wu, Richard Y J RYJ; Heilbron, Karl K; Ruskey, Jennifer A JA; Laurent, Sandra B SB; Blauwendraat, Cornelis C; Alam, Armaghan A; Arnulf, Isabelle I; Hu, Michele T M MTM; Dauvilliers, Yves Y; Högl, Birgit B; Toft, Mathias M; Bjørnarå, Kari Anne KA; Stefani, Ambra A; Holzknecht, Evi E; Monaca, Christelle Charley CC; Abril, Beatriz B; Plazzi, Giuseppe G; Antelmi, Elena E; Ferini-Strambi, Luigi L; Young, Peter P; Heidbreder, Anna A; Cochen De Cock, Valérie V; Mollenhauer, Brit B; Sixel-Döring, Friederike F; Trenkwalder, Claudia C; Sonka, Karel K; Kemlink, David D; Figorilli, Michela M; Puligheddu, Monica M; Dijkstra, Femke F; Viaene, Mineke M; Oertel, Wolfang W; Toffoli, Marco M; Gigli, Gian Luigi GL; Valente, Mariarosaria M; Gagnon, Jean-François JF; Nalls, Mike A MA; Singleton, Andrew B AB; , ; Desautels, Alex A; Montplaisir, Jacques Y JY; Cannon, Paul P; Ross, Owen A OA; Boeve, Bradley F BF; Dupré, Nicolas N; Fon, Edward A EA; Postuma, Ronald B RB; Pihlstrøm, Lasse L; Rouleau, Guy A GA; Gan-Or, Ziv Z
Publication Date: 2020-04

Variant appearance in text: rs2737024
PubMed Link: 31976583
Variant Present in the following documents:
  • Main text
View BVdb publication page



Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.

American Journal Of Human Genetics
McClymont, Sarah A SA; Hook, Paul W PW; Soto, Alexandra I AI; Reed, Xylena X; Law, William D WD; Kerans, Samuel J SJ; Waite, Eric L EL; Briceno, Nicole J NJ; Thole, Joey F JF; Heckman, Michael G MG; Diehl, Nancy N NN; Wszolek, Zbigniew K ZK; Moore, Cedric D CD; Zhu, Heng H; Akiyama, Jennifer A JA; Dickel, Diane E DE; Visel, Axel A; Pennacchio, Len A LA; Ross, Owen A OA; Beer, Michael A MA; McCallion, Andrew S AS
Publication Date: 2018-12-06

Variant appearance in text: rs2737024
PubMed Link: 30503521
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs2737024
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: rs2737024
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page