Varaico: Literature-Extracted Genetic Variants

Gene:XYLT1
Variant:p.F508_S509del1
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XYLT1

NM_022166.4:p.F508_S509del1

Associated Papers

SputOMICs identifies common and distinct markers in cystic fibrosis and chronic obstructive pulmonary disease.

Frey DL et al.

Scientific Reports, 2025

41436524 (PubMed )
Supplement: 41598_2025_32565_MOESM1_ESM.docx

Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance.

Wang Y et al.

The British Journal of Ophthalmology, 2023

36180177 (PubMed )
Supplement: bjo-2022-321511supp006.pdf

Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing.

Zheng J et al.

International Journal of Legal Medicine, 2018

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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."