FLT1 c.1436+3896C>T

Variant ID: 13-28997400-G-A

NM_002019.4(FLT1):c.1436+3896C>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis.

Frontiers In Pharmacology
Sales, Rahyssa Rodrigues RR; Nogueira, Bárbara Lisboa BL; Tosatti, Jéssica Abdo Gonçalves JAG; Gomes, Karina Braga KB; Luizon, Marcelo Rizzatti MR
Publication Date: 2021

Variant appearance in text: rs8002446
PubMed Link: 35126118
Variant Present in the following documents:
  • Main text
  • fphar-12-779497.pdf
View BVdb publication page



Genome-based therapeutic interventions for β-type hemoglobinopathies.

Human Genomics
Karamperis, Kariofyllis K; Tsoumpeli, Maria T MT; Kounelis, Fotios F; Koromina, Maria M; Mitropoulou, Christina C; Moutinho, Catia C; Patrinos, George P GP
Publication Date: 2021-06-05

Variant appearance in text: rs8002446
PubMed Link: 34090531
Variant Present in the following documents:
  • Main text
  • 40246_2021_Article_329.pdf
View BVdb publication page



Sepsis-associated acute respiratory distress syndrome in individuals of European ancestry: a genome-wide association study.

The Lancet. Respiratory Medicine
Guillen-Guio, Beatriz B; Lorenzo-Salazar, Jose M JM; Ma, Shwu-Fan SF; Hou, Pei-Chi PC; Hernandez-Beeftink, Tamara T; Corrales, Almudena A; García-Laorden, M Isabel MI; Jou, Jonathan J; Espinosa, Elena E; Muriel, Arturo A; Domínguez, David D; Lorente, Leonardo L; Martín, María M MM; Rodríguez-Gallego, Carlos C; Solé-Violán, Jordi J; Ambrós, Alfonso A; Carriedo, Demetrio D; Blanco, Jesús J; Añón, José M JM; Reilly, John P JP; Jones, Tiffanie K TK; Ittner, Caroline Ag CA; Feng, Rui R; Schöneweck, Franziska F; Kiehntopf, Michael M; Noth, Imre I; Scholz, Markus M; Brunkhorst, Frank M FM; Scherag, André A; Meyer, Nuala J NJ; Villar, Jesús J; Flores, Carlos C
Publication Date: 2020-03

Variant appearance in text: rs8002446
PubMed Link: 31982041
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pharmacogenomics of sickle cell disease: steps toward personalized medicine.

Pharmacogenomics And Personalized Medicine
Husain, Marium M; Hartman, Amber D AD; Desai, Payal P
Publication Date: 2017

Variant appearance in text: rs8002446
PubMed Link: 29089781
Variant Present in the following documents:
  • Main text
  • pgpm-10-261.pdf
View BVdb publication page



An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine.

Omics : A Journal Of Integrative Biology
Mnika, Khuthala K; Pule, Gift D GD; Dandara, Collet C; Wonkam, Ambroise A
Publication Date: 2016-10

Variant appearance in text: rs8002446
PubMed Link: 27636225
Variant Present in the following documents:
  • Main text
View BVdb publication page



Chiari malformation type I: a case-control association study of 58 developmental genes.

Plos One
Urbizu, Aintzane A; Toma, Claudio C; Poca, Maria A MA; Sahuquillo, Juan J; Cuenca-León, Ester E; Cormand, Bru B; Macaya, Alfons A
Publication Date: 2013

Variant appearance in text: rs8002446
PubMed Link: 23437350
Variant Present in the following documents:
  • Main text
  • pone.0057241.pdf
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: rs8002446
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page