Varaico: Literature-Extracted Genetic Variants

Gene:HBB
Variant:p.G26_E27insFs
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HBB

NM_000518.5:p.G26_E27insFs

Associated Papers

Active spread of β-thalassemia beyond the thalassemia belt: A study on a Russian population.

Shchemeleva E et al.

Clinical Genetics, 2025

Global distribution of β-thalassemia mutations: An update.

Rao E et al.

Gene, 2024

Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran.

Mousavi SS et al.

Biomed Research International, 2024

The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran.

Bazazzadegan N et al.

Hemoglobin, 2023

Rare and New Mutations of B-Globin in Azari Population of Iran, a Considerable Diversity.

Abbasali FH et al.

Balkan Journal of Medical Genetics : Bjmg, 2023

Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies.

Tamana S et al.

Elife, 2022

36453528 (PubMed )
Supplement: elife-79713-supp2.xlsx › Input-Full_dataset

Distribution of HBB Gene Mutations in the Kurdish Population of Ilam Province, West Iran.

Moradi K et al.

Hemoglobin, 2020

Molecular Characterization and Disease-Related Morbidities of β-Thalassemia Patients from the Northeastern Part of Iraq.

Amin S et al.

International Journal of General Medicine, 2020

The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran.

Alibakhshi R et al.

Hemoglobin, 2019

Frequency of α-Globin Gene Triplications and Coinheritance with β-Globin Gene Mutations in the Iranian Population.

Abedini SS et al.

Hemoglobin, 2018

The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran.

Jalilian M et al.

Hemoglobin, 2017

A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia.

Jiang F et al.

Hemoglobin, 2017

The spectrum of β-thalassemia mutations in Kermanshah Province in West Iran and its association with hematological parameters.

Mehrabi M et al.

Hemoglobin, 2013

Rapid identification of HBB gene mutations by high-resolution melting analysis.

Shih HC et al.

Clinical Biochemistry, 2009

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."