SNCA c.306+8669T>C

Variant ID: 4-90734728-A-G

NM_000345.3(SNCA):c.306+8669T>C

This variant was identified in 3 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: rs2119787
PubMed Link: 31804560
Variant Present in the following documents:
  • 41598_2019_Article_54865.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: rs2119787
PubMed Link: 28781905
Variant Present in the following documents:
  • Main text
  • PD2017-4318416.pdf
View BVdb publication page



SNCA variant associated with Parkinson disease and plasma alpha-synuclein level.

Archives Of Neurology
Mata, Ignacio F IF; Shi, Min M; Agarwal, Pinky P; Chung, Kathryn A KA; Edwards, Karen L KL; Factor, Stewart A SA; Galasko, Douglas R DR; Ginghina, Carmen C; Griffith, Alida A; Higgins, Donald S DS; Kay, Denise M DM; Kim, Hojoong H; Leverenz, James B JB; Quinn, Joseph F JF; Roberts, John W JW; Samii, Ali A; Snapinn, Katherine W KW; Tsuang, Debby W DW; Yearout, Dora D; Zhang, Jing J; Payami, Haydeh H; Zabetian, Cyrus P CP
Publication Date: 2010-11

Variant appearance in text: rs2119787
PubMed Link: 21060011
Variant Present in the following documents:
  • Main text
View BVdb publication page