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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:FXR2

Variant:p.D567insFs

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FXR2

NM_004860.4:p.D567insFs

hg38:chr17:7592723 T>TC

Associated Papers

FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum.

Mroczek M et al.

Journal of Medical Genetics, 2022

35393337 (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."