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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:KCNA3

Variant:p.F486insFs

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KCNA3

NM_002232.5:p.F486insFs

hg38:chr1:110673353 A>AC

Associated Papers

Rare FMR1 gene mutations causing fragile X syndrome: A review.

Sitzmann AF et al.

American Journal of Medical Genetics. Part A, 2018

29178241 (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."