Varaico: Literature-Extracted Genetic Variants

Gene:HBB
Variant:p.H93Y
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HBB

NM_000518.5:p.H93Y

Associated Papers

Anesthetic Management of a Patient With Hemoglobin M Disease Undergoing Laparoscopic Uterine Myomectomy: A Case Report.

You L et al.

Journal of Perianesthesia Nursing : Official Journal of the American Society of Perianesthesia Nurses, 2024

Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A review.

Thaker P et al.

International Journal of Laboratory Hematology, 2024

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

The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia.

Kim DS et al.

Yonsei Medical Journal, 2020

Hb-M Hyde Park: a rare cause of cyanosis arising from a de novo mutation.

Rastogi L et al.

Blood Research, 2020

Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia.

Nicolau M et al.

Annals of Hematology, 2019

Hereditary methemoglobinemia caused by Hb M-Hyde Park (Hb M-Akita) (HBB:c.277C > T; p.His93Tyr).

Schnedl WJ et al.

Wiener Klinische Wochenschrift, 2019

Distinctive mutation spectrum of the HBB gene in an urban eastern Indian population.

Sahoo SS et al.

Hemoglobin, 2014

[Determination of glycated hemoglobins (Hb A1c)].

Lahousen T et al.

Wiener Klinische Wochenschrift, 2002

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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."