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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:NOMO1

Variant:p.Q482Q

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NOMO1

NM_014287.4:p.Q482Q

hg38:chr16:14864635 G>A

Associated Papers

Prevalence of pendrin defects in sudanese families with congenital hypothyroidism.

Islam MS et al.

Endocrine, 2025

40956475 (PubMed )

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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."