Varaico: Literature-Extracted Genetic Variants

Gene:FGF23
Variant:p.R176G
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FGF23

NM_020638.3:p.R176G

Associated Papers

A case of autosomal dominant hypophosphatemic rickets.

Takishima S et al.

Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology, 2025

Congenital hypophosphataemia in adults: determinants of bone turnover markers and amelioration of renal phosphate wasting following total parathyroidectomy.

McKenna MJ et al.

Journal of Bone and Mineral Metabolism, 2019

Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets.

Guven A et al.

Clinical Endocrinology, 2017

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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."