SNCA c.306+13795T>C

Variant ID: 4-90729602-A-G

NM_000345.3(SNCA):c.306+13795T>C

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Common genetic variants associated with Parkinson's disease display widespread signature of epigenetic plasticity.

Scientific Reports
Sharma, Amit A; Osato, Naoki N; Liu, Hongde H; Asthana, Shailendra S; Dakal, Tikam Chand TC; Ambrosini, Giovanna G; Bucher, Philipp P; Schmitt, Ina I; Wüllner, Ullrich U
Publication Date: 2019-12-05

Variant appearance in text: rs2197120
PubMed Link: 31804560
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_54865.pdf
View BVdb publication page



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: rs2197120
PubMed Link: 29730891
Variant Present in the following documents:
  • Main text
  • MGG3-6-565.pdf
View BVdb publication page



Genetic Variants in SNCA and the Risk of Sporadic Parkinson's Disease and Clinical Outcomes: A Review.

Parkinson'S Disease
Campêlo, Clarissa Loureiro das Chagas CLDC; Silva, Regina Helena RH
Publication Date: 2017

Variant appearance in text: rs2197120
PubMed Link: 28781905
Variant Present in the following documents:
  • Main text
  • PD2017-4318416.pdf
View BVdb publication page



Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.

Molecular Psychiatry
Desikan, R S RS; Schork, A J AJ; Wang, Y Y; Witoelar, A A; Sharma, M M; McEvoy, L K LK; Holland, D D; Brewer, J B JB; Chen, C-H CH; Thompson, W K WK; Harold, D D; Williams, J J; Owen, M J MJ; O'Donovan, M C MC; Pericak-Vance, M A MA; Mayeux, R R; Haines, J L JL; Farrer, L A LA; Schellenberg, G D GD; Heutink, P P; Singleton, A B AB; Brice, A A; Wood, N W NW; Hardy, J J; Martinez, M M; Choi, S H SH; DeStefano, A A; Ikram, M A MA; Bis, J C JC; Smith, A A; Fitzpatrick, A L AL; Launer, L L; van Duijn, C C; Seshadri, S S; Ulstein, I D ID; Aarsland, D D; Fladby, T T; Djurovic, S S; Hyman, B T BT; Snaedal, J J; Stefansson, H H; Stefansson, K K; Gasser, T T; Andreassen, O A OA; Dale, A M AM; ,
Publication Date: 2015-12

Variant appearance in text: rs2197120
PubMed Link: 25687773
Variant Present in the following documents:
  • Main text
  • nihms654369.pdf
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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: rs2197120
PubMed Link: 23384371
Variant Present in the following documents:
  • Main text
View BVdb publication page



SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population.

Parkinsonism & Related Disorders
Trotta, Luca L; Guella, Ilaria I; Soldà, Giulia G; Sironi, Francesca F; Tesei, Silvana S; Canesi, Margherita M; Pezzoli, Gianni G; Goldwurm, Stefano S; Duga, Stefano S; Asselta, Rosanna R
Publication Date: 2012-03

Variant appearance in text: rs2197120
PubMed Link: 22104010
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: rs2197120
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page