CDKAL1 c.743-32787C>T

Variant ID: 6-20922863-C-T

NM_017774.3(CDKAL1):c.743-32787C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association study of sporadic brain arteriovenous malformations.

Journal Of Neurology, Neurosurgery, And Psychiatry
Weinsheimer, Shantel S; Bendjilali, Nasrine N; Nelson, Jeffrey J; Guo, Diana E DE; Zaroff, Jonathan G JG; Sidney, Stephen S; McCulloch, Charles E CE; Al-Shahi Salman, Rustam R; Berg, Jonathan N JN; Koeleman, Bobby P C BP; Simon, Matthias M; Bostroem, Azize A; Fontanella, Marco M; Sturiale, Carmelo L CL; Pola, Roberto R; Puca, Alfredo A; Lawton, Michael T MT; Young, William L WL; Pawlikowska, Ludmila L; Klijn, Catharina J M CJ; Kim, Helen H; ,
Publication Date: 2016-09

Variant appearance in text: rs9460577
PubMed Link: 26818729
Variant Present in the following documents:
  • Main text
View BVdb publication page