Varaico: Literature-Extracted Genetic Variants

Gene:SNX14
Variant:p.D155fs
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SNX14

NM_153816.6:p.D155fs

Associated Papers

Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report.

Levchenko O et al.

Frontiers in Genetics, 2023

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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."