Varaico: Literature-Extracted Genetic Variants

Gene:HBB
Variant:p.E23G
Back to variants list

HBB

NM_000518.5:p.E23G

Associated Papers

Rare Coexistence of Hemoglobin D-Iran and Hemoglobin S in a Case from Central India.

Rani P et al.

Hemoglobin, 2025

Genotypic and phenotypic characterization of rare globin variants in Northern Guangxi, China.

Yang WJ et al.

Frontiers in Immunology, 2025

Compound heterozygous with Hb G-Taipei and Hb Lepore-Boston-Washington: An unexpected finding triggered by HbA1c measurement.

Li Y et al.

Practical Laboratory Medicine, 2024

Screening for thalassemia carriers among the Han population of childbearing age in Southwestern of China.

Du Y et al.

Frontiers in Genetics, 2024

Identification of Novel Hb Guiyang [HBA2: c.151C > A α2 50 (CE8) His- Asn] and Phenotype- Genotype Correlation of Abnormal Hemoglobins in Guizhou, Southwest China.

Chen YP et al.

Journal of Blood Medicine, 2024

Differential Effects on HbA1c Detection by HPLC and Capillary Electrophoresis in Five Types of Hb Variants in China.

Wei L et al.

Laboratory Medicine, 2023

Evaluation of interference from 16 hemoglobin variants on hemoglobin A1c measurement by five methods.

Yang X et al.

Scandinavian Journal of Clinical and Laboratory Investigation, 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

Molecular epidemiological investigation of abnormal hemoglobin in Shaokwan region, southern China.

Yang H et al.

Hematology (amsterdam, Netherlands), 2022

Use of Capillary Electrophoresis Migration Position for the Presumptive Identification of Hemoglobin Variants Prevalent in China.

Xu M et al.

Hemoglobin, 2022

Identification of Hemoglobin Variants Prevalent in China and Their Effects on Hemoglobin A1c Measurements.

Xu A et al.

American Journal of Clinical Pathology, 2022

Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China.

Luo H et al.

Frontiers in Genetics, 2022

Molecular characterization of hemoglobinopathies and thalassemias in Northern Guangdong Province, China.

Ma Z et al.

Medicine, 2021

Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.

Cirulli ET et al.

Nature Communications, 2020

31992710 (PubMed )
Supplement: 41467_2020_14288_MOESM1_ESM.pdf

Effects of common hemoglobin variants on HbA1c measurements in China: results for α- and β-globin variants measured by six methods.

Xu A et al.

Clinical Chemistry and Laboratory Medicine, 2018

Molecular Epidemiological Survey of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassemia in Uygur and Kazak Ethnic Groups in Xinjiang, Northwest China.

Han L et al.

Hemoglobin, 2016

Genetic heterogeneity of the β-globin gene in various geographic populations of Yunnan in southwestern China.

Zhang J et al.

Plos One, 2015

Prevalence and molecular characterization of structural hemoglobin variants in the Dongguan region of Guangdong province, southern China.

Lou JW et al.

Hemoglobin, 2014

Molecular epidemiological survey of hemoglobinopathies in the Wuxi region of Jiangsu Province, eastern China.

Lin M et al.

Hemoglobin, 2013

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."