Varaico: Literature-Extracted Genetic Variants

Gene:FCN1
Variant:p.T150M
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FCN1

NM_002003.5:p.T150M

Associated Papers

Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation.

Leimi L et al.

Frontiers in Immunology, 2023

37771589 (PubMed )
Supplement: DataSheet_2.pdf

Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.

Ostrowski J et al.

Scientific Reports, 2016

28008999 (PubMed )
Supplement: srep39831-s2.xls › Table_S7

Exome analysis of a family with pleiotropic congenital heart disease.

Arrington CB et al.

Circulation. Cardiovascular Genetics, 2012

Non-synonymous polymorphisms in the FCN1 gene determine ligand-binding ability and serum levels of M-ficolin.

Ammitzbøll CG et al.

Plos One, 2012

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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."