SNCA c.307-14366G>A

Variant ID: 4-90664794-C-T

NM_000345.3(SNCA):c.307-14366G>A

This variant was identified in 16 publications

View GRCh38 version.




Publications:


Genetics of Multiple System Atrophy and Progressive Supranuclear Palsy: A Systemized Review of the Literature.

International Journal Of Molecular Sciences
Bougea, Anastasia A
Publication Date: 2023-03-09

Variant appearance in text: rs3822086
PubMed Link: 36982356
Variant Present in the following documents:
  • Main text
  • ijms-24-05281.pdf
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The Genetic Landscape of Parkinsonism-Related Dystonias and Atypical Parkinsonism-Related Syndromes.

International Journal Of Molecular Sciences
Diez-Fairen, Monica M; Alvarez Jerez, Pilar P; Berghausen, Joos J; Bandres-Ciga, Sara S
Publication Date: 2021-07-28

Variant appearance in text: rs3822086
PubMed Link: 34360863
Variant Present in the following documents:
  • Main text
  • ijms-22-08100.pdf
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A systematic review of associations between common SNCA variants and clinical heterogeneity in Parkinson's disease.

Npj Parkinson'S Disease
Pedersen, Camilla Christina CC; Lange, Johannes J; Førland, Marthe Gurine Gunnarsdatter MGG; Macleod, Angus D AD; Alves, Guido G; Maple-Grødem, Jodi J
Publication Date: 2021-07-01

Variant appearance in text: rs3822086
PubMed Link: 34210990
Variant Present in the following documents:
  • 41531_2021_196_MOESM1_ESM.pdf
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MicroRNAs Dysregulation and Metabolism in Multiple System Atrophy.

Frontiers In Neuroscience
Xiang, Chunchen C; Han, Shunchang S; Nao, Jianfei J; Cong, Shuyan S
Publication Date: 2019

Variant appearance in text: rs3822086
PubMed Link: 31680837
Variant Present in the following documents:
  • Main text
  • fnins-13-01103.pdf
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Parkinson's disease in China: a forty-year growing track of bedside work.

Translational Neurodegeneration
Li, Gen G; Ma, Jianfang J; Cui, Shishuang S; He, Yixi Y; Xiao, Qin Q; Liu, Jun J; Chen, Shengdi S
Publication Date: 2019

Variant appearance in text: rs3822086
PubMed Link: 31384434
Variant Present in the following documents:
  • Main text
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Cross-examining candidate genes implicated in multiple system atrophy.

Acta Neuropathologica Communications
Katzeff, Jared S JS; Phan, Katherine K; Purushothuman, Sivaraman S; Halliday, Glenda M GM; Kim, Woojin Scott WS
Publication Date: 2019-07-24

Variant appearance in text: rs3822086
PubMed Link: 31340844
Variant Present in the following documents:
  • Main text
  • 40478_2019_Article_769.pdf
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A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease.

Frontiers In Molecular Neuroscience
Zhang, Yuan Y; Shu, Li L; Sun, Qiying Q; Pan, Hongxu H; Guo, Jifeng J; Tang, Beisha B
Publication Date: 2018

Variant appearance in text: rs3822086
PubMed Link: 30410434
Variant Present in the following documents:
  • Main text
  • fnmol-11-00391.pdf
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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: rs3822086
PubMed Link: 28781905
Variant Present in the following documents:
  • Main text
  • PD2017-4318416.pdf
View BVdb publication page



A genome-wide association study in multiple system atrophy.

Neurology
Sailer, Anna A; Scholz, Sonja W SW; Nalls, Michael A MA; Schulte, Claudia C; Federoff, Monica M; Price, T Ryan TR; Lees, Andrew A; Ross, Owen A OA; Dickson, Dennis W DW; Mok, Kin K; Mencacci, Niccolo E NE; Schottlaender, Lucia L; Chelban, Viorica V; Ling, Helen H; O'Sullivan, Sean S SS; Wood, Nicholas W NW; Traynor, Bryan J BJ; Ferrucci, Luigi L; Federoff, Howard J HJ; Mhyre, Timothy R TR; Morris, Huw R HR; Deuschl, Günther G; Quinn, Niall N; Widner, Hakan H; Albanese, Alberto A; Infante, Jon J; Bhatia, Kailash P KP; Poewe, Werner W; Oertel, Wolfgang W; Höglinger, Günter U GU; Wüllner, Ullrich U; Goldwurm, Stefano S; Pellecchia, Maria Teresa MT; Ferreira, Joaquim J; Tolosa, Eduardo E; Bloem, Bastiaan R BR; Rascol, Olivier O; Meissner, Wassilios G WG; Hardy, John A JA; Revesz, Tamas T; Holton, Janice L JL; Gasser, Thomas T; Wenning, Gregor K GK; Singleton, Andrew B AB; Houlden, Henry H; ,
Publication Date: 2016-10-11

Variant appearance in text: rs3822086
PubMed Link: 27629089
Variant Present in the following documents:
  • Main text
  • NEUROLOGY2016719088.pdf
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Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression.

Neurobiology Of Aging
Davis, Albert A AA; Andruska, Kristin M KM; Benitez, Bruno A BA; Racette, Brad A BA; Perlmutter, Joel S JS; Cruchaga, Carlos C
Publication Date: 2016-01

Variant appearance in text: rs3822086
PubMed Link: 26601739
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.

Plos One
Chen, YongPing Y; Wei, Qian-Qian QQ; Ou, RuWei R; Cao, Bei B; Chen, XuePing X; Zhao, Bi B; Guo, XiaoYan X; Yang, Yuan Y; Chen, Ke K; Wu, Ying Y; Song, Wei W; Shang, Hui-Fang HF
Publication Date: 2015

Variant appearance in text: rs3822086
PubMed Link: 26208350
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis.

Plos One
Yang, Xinglong X; Xi, Jing J; Zhao, Quanzhen Q; Jia, Hua H; An, Ran R; Liu, Zhuolin Z; Xu, Yanming Y
Publication Date: 2015

Variant appearance in text: rs3822086
PubMed Link: 26098829
Variant Present in the following documents:
  • Main text
  • pone.0130970.pdf
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The neurogenetics of atypical parkinsonian disorders.

Seminars In Neurology
Fogel, Brent L BL; Clark, Mary C MC; Geschwind, Daniel H DH
Publication Date: 2014-04

Variant appearance in text: rs3822086
PubMed Link: 24963681
Variant Present in the following documents:
  • Main text
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Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.

Plos One
Al-Chalabi, Ammar A; Dürr, Alexandra A; Wood, Nicholas W NW; Parkinson, Michael H MH; Camuzat, Agnes A; Hulot, Jean-Sébastien JS; Morrison, Karen E KE; Renton, Alan A; Sussmuth, Sigurd D SD; Landwehrmeyer, Bernhard G BG; Ludolph, Albert A; Agid, Yves Y; Brice, Alexis A; Leigh, P Nigel PN; Bensimon, Gilbert G; ,
Publication Date: 2009-09-22

Variant appearance in text: rs3822086
PubMed Link: 19771175
Variant Present in the following documents:
  • Main text
  • pone.0007114.pdf
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Linkage disequilibrium patterns and tagSNP transferability among European populations.

American Journal Of Human Genetics
Mueller, Jakob C JC; Lõhmussaar, Elin E; Mägi, Reedik R; Remm, Maido M; Bettecken, Thomas T; Lichtner, Peter P; Biskup, Saskia S; Illig, Thomas T; Pfeufer, Arne A; Luedemann, Jan J; Schreiber, Stefan S; Pramstaller, Peter P; Pichler, Irene I; Romeo, Giovanni G; Gaddi, Anthony A; Testa, Alessandra A; Wichmann, Heinz-Erich HE; Metspalu, Andres A; Meitinger, Thomas T
Publication Date: 2005-03

Variant appearance in text: rs3822086
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page