Varaico: Literature-Extracted Genetic Variants

Gene:SCD5
Variant:p.W209S
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SCD5

NM_001037582.3:p.W209S

Associated Papers

Whole exome sequencing identifies SCD5 as a novel causative gene for autosomal dominant nonsyndromic deafness.

Lu X et al.

European Journal of Medical Genetics, 2020

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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."