SNCA c.306+39644A>G

Variant ID: 4-90703753-T-C

NM_000345.3(SNCA):c.306+39644A>G

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: rs10018362
PubMed Link: 31804560
Variant Present in the following documents:
  • 41598_2019_Article_54865.pdf
View BVdb publication page



Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.

Molecular Neurobiology
Zucchelli, Silvia S; Fedele, Stefania S; Vatta, Paolo P; Calligaris, Raffaella R; Heutink, Peter P; Rizzu, Patrizia P; Itoh, Masayoshi M; Persichetti, Francesca F; Santoro, Claudio C; Kawaji, Hideya H; Lassmann, Timo T; Hayashizaki, Yoshihide Y; Carninci, Piero P; Forrest, Alistair R R ARR; , ; Gustincich, Stefano S
Publication Date: 2019-08

Variant appearance in text: rs10018362
PubMed Link: 30610612
Variant Present in the following documents:
  • 12035_2018_Article_1465.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: rs10018362
PubMed Link: 28781905
Variant Present in the following documents:
  • Main text
  • PD2017-4318416.pdf
View BVdb publication page