SNCA c.307-33850T>C

Variant ID: 4-90684278-A-G

NM_000345.3(SNCA):c.307-33850T>C

This variant was identified in 2 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: rs10516845
PubMed Link: 34210990
Variant Present in the following documents:
  • 41531_2021_196_MOESM1_ESM.pdf
View BVdb publication page



Familial genes in sporadic disease: common variants of alpha-synuclein gene associate with Parkinson's disease.

Mechanisms Of Ageing And Development
Ross, Owen A OA; Gosal, David D; Stone, Jeremy T JT; Lincoln, Sarah J SJ; Heckman, Michael G MG; Irvine, G Brent GB; Johnston, Janet A JA; Gibson, J Mark JM; Farrer, Matthew J MJ; Lynch, Timothy T
Publication Date: 2007

Variant appearance in text: rs10516845
PubMed Link: 17531291
Variant Present in the following documents:
  • Main text
View BVdb publication page