KIF11 c.388-189T>C

Variant ID: 10-94368588-T-C

NM_004523.3(KIF11):c.388-189T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease.

Neurology
Zou, F F; Carrasquillo, M M MM; Pankratz, V S VS; Belbin, O O; Morgan, K K; Allen, M M; Wilcox, S L SL; Ma, L L; Walker, L P LP; Kouri, N N; Burgess, J D JD; Younkin, L H LH; Younkin, Samuel G SG; Younkin, C S CS; Bisceglio, G D GD; Crook, J E JE; Dickson, D W DW; Petersen, R C RC; Graff-Radford, N N; Younkin, Steven G SG; Ertekin-Taner, N N
Publication Date: 2010-02-09

Variant appearance in text: rs10882088
PubMed Link: 20142614
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs10882088
PubMed Link: 20070850
Variant Present in the following documents:
  • Main text
View BVdb publication page