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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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