SNCA c.306+11688T>C

Variant ID: 4-90731709-A-G

NM_000345.3(SNCA):c.306+11688T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.

Annals Of Human Genetics
Edwards, Todd L TL; Scott, William K WK; Almonte, Cherylyn C; Burt, Amber A; Powell, Eric H EH; Beecham, Gary W GW; Wang, Liyong L; Züchner, Stephan S; Konidari, Ioanna I; Wang, Gaofeng G; Singer, Carlos C; Nahab, Fatta F; Scott, Burton B; Stajich, Jeffrey M JM; Pericak-Vance, Margaret M; Haines, Jonathan J; Vance, Jeffery M JM; Martin, Eden R ER
Publication Date: 2010-03

Variant appearance in text: rs1866995
PubMed Link: 20070850
Variant Present in the following documents:
  • Main text
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