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