ITGAV c.317-8566A>G

Variant ID: 2-187478500-A-G

NM_002210.4(ITGAV):c.317-8566A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The search for genetic modifiers of disease severity in the β-hemoglobinopathies.

Cold Spring Harbor Perspectives In Medicine
Lettre, Guillaume G
Publication Date: 2012-10-01

Variant appearance in text: rs3768780
PubMed Link: 23028136
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: rs3768780
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page