SNCA c.121+759T>C

Variant ID: 4-90755939-A-G

NM_000345.3(SNCA):c.121+759T>C

This variant was identified in 5 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: rs2583985
PubMed Link: 29730891
Variant Present in the following documents:
  • Main text
  • MGG3-6-565.pdf
View BVdb publication page



Neuroimaging in psychiatric pharmacogenetics research: the promise and pitfalls.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology
Falcone, Mary M; Smith, Ryan M RM; Chenoweth, Meghan J MJ; Bhattacharjee, Abesh Kumar AK; Kelsoe, John R JR; Tyndale, Rachel F RF; Lerman, Caryn C; ,
Publication Date: 2013-11

Variant appearance in text: rs2583985
PubMed Link: 23793356
Variant Present in the following documents:
  • Main text
View BVdb publication page



Small cell ovarian carcinoma: genomic stability and responsiveness to therapeutics.

Orphanet Journal Of Rare Diseases
Gamwell, Lisa F LF; Gambaro, Karen K; Merziotis, Maria M; Crane, Colleen C; Arcand, Suzanna L SL; Bourada, Valerie V; Davis, Christopher C; Squire, Jeremy A JA; Huntsman, David G DG; Tonin, Patricia N PN; Vanderhyden, Barbara C BC
Publication Date: 2013-02-21

Variant appearance in text: rs2583985
PubMed Link: 23433318
Variant Present in the following documents:
  • Main text
  • 1750-1172-8-33.pdf
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: rs2583985
PubMed Link: 23384371
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.

Annals Of Human Genetics
Edwards, Todd L TL; Scott, William K WK; Almonte, Cherylyn C; Burt, Amber A; Powell, Eric H EH; Beecham, Gary W GW; Wang, Liyong L; Züchner, Stephan S; Konidari, Ioanna I; Wang, Gaofeng G; Singer, Carlos C; Nahab, Fatta F; Scott, Burton B; Stajich, Jeffrey M JM; Pericak-Vance, Margaret M; Haines, Jonathan J; Vance, Jeffery M JM; Martin, Eden R ER
Publication Date: 2010-03

Variant appearance in text: rs2583985
PubMed Link: 20070850
Variant Present in the following documents:
  • Main text
View BVdb publication page