Varaico: Literature-Extracted Genetic Variants

Gene:IFNAR1
Variant:p.V225Splc
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IFNAR1

NM_000629.3:p.V225Splc

Associated Papers

Null IFNAR1 and IFNAR2 alleles are surprisingly common in the Pacific and Arctic.

Meyts I

The Journal of Experimental Medicine, 2022

Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome.

Abolhassani H et al.

Journal of Clinical Immunology, 2022

A Case of Autosomal Recessive Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency with Severe COVID-19.

Khanmohammadi S et al.

Journal of Clinical Immunology, 2022

The role of host genetics in susceptibility to severe viral infections in humans and insights into host genetics of severe COVID-19: A systematic review.

Elhabyan A et al.

Virus Research, 2020

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines.

Hernandez N et al.

The Journal of Experimental Medicine, 2019

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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."