SNCA c.307-23342T>G

Variant ID: 4-90673770-A-C

NM_000345.3(SNCA):c.307-23342T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Imputation and Reanalysis of ExomeChip Data Identifies Novel, Conditional and Joint Genetic Effects on Parkinson's Disease Risk.

Genes
Rodrigo, Linduni M LM; Nyholt, Dale R DR
Publication Date: 2021-05-04

Variant appearance in text: rs356167
PubMed Link: 34064523
Variant Present in the following documents:
  • Main text
  • genes-12-00689.pdf
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: rs356167
PubMed Link: 15637659
Variant Present in the following documents:
  • Main text
View BVdb publication page