Varaico: Literature-Extracted Genetic Variants

Gene:FSCN2
Variant:p.S147I
Back to variants list

FSCN2

NM_012418.4:p.S147I

Associated Papers

Allele frequency analysis of variants reported to cause autosomal dominant inherited retinal diseases question the involvement of 19% of genes and 10% of reported pathogenic variants.

Hanany M et al.

Journal of Medical Genetics, 2019

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."