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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:CLDN9

Variant:p.L29delFs

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CLDN9

NM_020982.4:p.L29delFs

hg38:chr16:3013447 CT>C

Associated Papers

A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.

Sineni CJ et al.

Human Genetics, 2019

31175426 (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."