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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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