SNCA c.307-41109A>G

Variant ID: 4-90691537-T-C

NM_000345.3(SNCA):c.307-41109A>G

This variant was identified in 9 publications

View GRCh38 version.




Publications:


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: rs356188
PubMed Link: 27478013
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs356188
PubMed Link: 23384371
Variant Present in the following documents:
  • Main text
View BVdb publication page



Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain.

Parkinson'S Disease
Dumitriu, Alexandra A; Moser, Carlee C; Hadzi, Tiffany C TC; Williamson, Sally L SL; Pacheco, Christopher D CD; Hendricks, Audrey E AE; Latourelle, Jeanne C JC; Wilk, Jemma B JB; Destefano, Anita L AL; Myers, Richard H RH
Publication Date: 2012

Variant appearance in text: rs356188
PubMed Link: 22530163
Variant Present in the following documents:
  • Main text
  • PD2012-614212.pdf
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Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study.

Human Molecular Genetics
Dumitriu, Alexandra A; Pacheco, Chris D CD; Wilk, Jemma B JB; Strathearn, Katherine E KE; Latourelle, Jeanne C JC; Goldwurm, Stefano S; Pezzoli, Gianni G; Rochet, Jean-Christophe JC; Lindquist, Susan S; Myers, Richard H RH
Publication Date: 2011-04-15

Variant appearance in text: rs356188
PubMed Link: 21258085
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study confirms extant PD risk loci among the Dutch.

European Journal Of Human Genetics : Ejhg
Simón-Sánchez, Javier J; van Hilten, Jacobus J JJ; van de Warrenburg, Bart B; Post, Bart B; Berendse, Henk W HW; Arepalli, Sampath S; Hernandez, Dena G DG; de Bie, Rob M A RM; Velseboer, Daan D; Scheffer, Hans H; Bloem, Bas B; van Dijk, Karin D KD; Rivadeneira, Fernando F; Hofman, Albert A; Uitterlinden, André G AG; Rizzu, Patrizia P; Bochdanovits, Zoltan Z; Singleton, Andrew B AB; Heutink, Peter P
Publication Date: 2011-06

Variant appearance in text: rs356188
PubMed Link: 21248740
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

Nature Genetics
Hamza, Taye H TH; Zabetian, Cyrus P CP; Tenesa, Albert A; Laederach, Alain A; Montimurro, Jennifer J; Yearout, Dora D; Kay, Denise M DM; Doheny, Kimberly F KF; Paschall, Justin J; Pugh, Elizabeth E; Kusel, Victoria I VI; Collura, Randall R; Roberts, John J; Griffith, Alida A; Samii, Ali A; Scott, William K WK; Nutt, John J; Factor, Stewart A SA; Payami, Haydeh H
Publication Date: 2010-09

Variant appearance in text: rs356188
PubMed Link: 20711177
Variant Present in the following documents:
  • NIHMS222438-supplement-1.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: rs356188
PubMed Link: 19771175
Variant Present in the following documents:
  • Main text
  • pone.0007114.pdf
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Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

Human Genetics
Pankratz, Nathan N; Wilk, Jemma B JB; Latourelle, Jeanne C JC; DeStefano, Anita L AL; Halter, Cheryl C; Pugh, Elizabeth W EW; Doheny, Kimberly F KF; Gusella, James F JF; Nichols, William C WC; Foroud, Tatiana T; Myers, Richard H RH; ,
Publication Date: 2009-01

Variant appearance in text: rs356188
PubMed Link: 18985386
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: rs356188
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page