Varaico: Literature-Extracted Genetic Variants

Gene:NKX2-1
Variant:p.L25F
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NKX2-1

NM_001079668.3:p.L25F

Associated Papers

Functional Noncoding Variants in a TTTG Microsatellite on Chromosome 15q26.1 Are a Common Genetic Etiology of Congenital Hypothyroidism with Thyroid Gland in situ.

Shima H et al.

Hormone Research in Paediatrics, 2025

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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."