BCLAF1 c.-115+1501G>A

Variant ID: 6-136609350-C-T

NM_014739.3(BCLAF1):c.-115+1501G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Germline variation in apoptosis pathway genes and risk of non-Hodgkin's lymphoma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Kelly, Jennifer L JL; Novak, Anne J AJ; Fredericksen, Zachary S ZS; Liebow, Mark M; Ansell, Stephen M SM; Dogan, Ahmet A; Wang, Alice H AH; Witzig, Thomas E TE; Call, Timothy G TG; Kay, Neil E NE; Habermann, Thomas M TM; Slager, Susan L SL; Cerhan, James R JR
Publication Date: 2010-11

Variant appearance in text: rs703193
PubMed Link: 20855536
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs703193
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
View BVdb publication page



Admixture mapping provides evidence of association of the VNN1 gene with hypertension.

Plos One
Zhu, Xiaofeng X; Cooper, Richard S RS
Publication Date: 2007-11-28

Variant appearance in text: rs703193
PubMed Link: 18043751
Variant Present in the following documents:
  • Main text
  • pone.0001244.pdf
View BVdb publication page