SNCA c.306+3858G>T

Variant ID: 4-90739539-C-A

NM_000345.3(SNCA):c.306+3858G>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Alpha-synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3'UTR.

Molecular Genetics & Genomic Medicine
Barrie, Elizabeth S ES; Lee, Sung-Ha SH; Frater, John T JT; Kataki, Maria M; Scharre, Douglas W DW; Sadee, Wolfgang W
Publication Date: 2018-05-06

Variant appearance in text: rs1812923
PubMed Link: 29730891
Variant Present in the following documents:
  • Main text
  • MGG3-6-565.pdf
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Alpha-synuclein (SNCA) polymorphisms exert protective effects on memory after mild traumatic brain injury.

Neuroscience Letters
Shee, Kevin K; Lucas, Alexandra A; Flashman, Laura A LA; Nho, Kwangsik K; Tsongalis, Gregory J GJ; McDonald, Brenna C BC; Saykin, Andrew J AJ; McAllister, Thomas W TW; Rhodes, C Harker CH
Publication Date: 2016-09-06

Variant appearance in text: rs1812923
PubMed Link: 27478013
Variant Present in the following documents:
  • Main text
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Genetic variation in the alpha synuclein gene (SNCA) is associated with BOLD response to alcohol cues.

Journal Of Studies On Alcohol And Drugs
Wilcox, Claire E CE; Claus, Eric D ED; Blaine, Sara K SK; Morgan, Marilee M; Hutchison, Kent E KE
Publication Date: 2013-03

Variant appearance in text: rs1812923
PubMed Link: 23384371
Variant Present in the following documents:
  • Main text
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Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12

Variant appearance in text: rs1812923
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
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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: rs1812923
PubMed Link: 19771175
Variant Present in the following documents:
  • Main text
  • pone.0007114.pdf
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Genetic susceptibility in Parkinson's disease.

Biochimica Et Biophysica Acta
Bras, Jose Miguel JM; Singleton, Andrew A
Publication Date: 2009-07

Variant appearance in text: rs1812923
PubMed Link: 19063963
Variant Present in the following documents:
  • Main text
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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: rs1812923
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page