SNCA c.306+6070C>T

Variant ID: 4-90737327-G-A

NM_000345.3(SNCA):c.306+6070C>T

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis.

Frontiers In Psychiatry
Yin, Bian B; Wang, Xinpei X; Huang, Tao T; Jia, Jinzhu J
Publication Date: 2022

Variant appearance in text: rs974711
PubMed Link: 35898629
Variant Present in the following documents:
  • Main text
  • fpsyt-13-910432.pdf
View BVdb publication page



Genetic Architecture and Molecular, Imaging and Prodromic Markers in Dementia with Lewy Bodies: State of the Art, Opportunities and Challenges.

International Journal Of Molecular Sciences
Combi, Romina R; Salsone, Maria M; Villa, Chiara C; Ferini-Strambi, Luigi L
Publication Date: 2021-04-12

Variant appearance in text: rs974711
PubMed Link: 33921279
Variant Present in the following documents:
  • Main text
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: rs974711
PubMed Link: 30610612
Variant Present in the following documents:
  • 12035_2018_Article_1465.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: rs974711
PubMed Link: 29730891
Variant Present in the following documents:
  • Main text
  • MGG3-6-565.pdf
View BVdb publication page



Item-level analyses reveal genetic heterogeneity in neuroticism.

Nature Communications
Nagel, Mats M; Watanabe, Kyoko K; Stringer, Sven S; Posthuma, Danielle D; van der Sluis, Sophie S
Publication Date: 2018-03-02

Variant appearance in text: rs974711
PubMed Link: 29500382
Variant Present in the following documents:
  • 41467_2018_3242_MOESM2_ESM.pdf
View BVdb publication page