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TOX c.1392+2849T>C
Variant ID: 8-59725048-A-G
NM_014729.2(
TOX
):c.1392+2849T>C
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: rs2693430
PubMed Link:
35126118
Variant Present in the following documents:
Main text
fphar-12-779497.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: rs2693430
PubMed Link:
27636225
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: rs2693430
PubMed Link:
20401335
Variant Present in the following documents:
Main text
gei-2-2009-023.pdf
View BVdb publication page