SNCA c.164-2168C>T

Variant ID: 4-90745707-G-A

NM_000345.3(SNCA):c.164-2168C>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


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: rs2737012
PubMed Link: 34210990
Variant Present in the following documents:
  • 41531_2021_196_MOESM1_ESM.pdf
View BVdb publication page



Genetic Risk Factors for Essential Tremor: A Review.

Tremor And Other Hyperkinetic Movements (New York, N.Y.)
Siokas, Vasileios V; Aloizou, Athina-Maria AM; Tsouris, Zisis Z; Liampas, Ioannis I; Aslanidou, Paraskevi P; Dastamani, Metaxia M; Brotis, Alexandros G AG; Bogdanos, Dimitrios P DP; Hadjigeorgiou, Georgios M GM; Dardiotis, Efthimios E
Publication Date: 2020-06-11

Variant appearance in text: rs2737012
PubMed Link: 32775018
Variant Present in the following documents:
  • tohm-10-1-67-s2.pdf
View BVdb publication page



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: rs2737012
PubMed Link: 31804560
Variant Present in the following documents:
  • 41598_2019_Article_54865.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: rs2737012
PubMed Link: 28781905
Variant Present in the following documents:
  • Main text
  • PD2017-4318416.pdf
View BVdb publication page



Evaluation of the role of SNCA variants in survival without neurological disease.

Plos One
Heckman, Michael G MG; Soto-Ortolaza, Alexandra I AI; Diehl, Nancy N NN; Carrasquillo, Minerva M MM; Uitti, Ryan J RJ; Wszolek, Zbigniew K ZK; Graff-Radford, Neill R NR; Ross, Owen A OA
Publication Date: 2012

Variant appearance in text: rs2737012
PubMed Link: 22912757
Variant Present in the following documents:
  • Main text
  • pone.0042877.pdf
View BVdb publication page



Genetic variants of α-synuclein are not associated with essential tremor.

Movement Disorders : Official Journal Of The Movement Disorder Society
Ross, Owen A OA; Conneely, Karen N KN; Wang, Tao T; Vilarino-Guell, Carles C; Soto-Ortolaza, Alexandra I AI; Rajput, Alex A; Wszolek, Zbigniew K ZK; Uitti, Ryan J RJ; Louis, Elan D ED; Clark, Lorraine N LN; Farrer, Matthew J MJ; Testa, Claudia M CM
Publication Date: 2011-12

Variant appearance in text: rs2737012
PubMed Link: 22025277
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs2737012
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page