FIGURE
Fig. 1
- ID
- ZDB-FIG-250717-26
- Publication
- Charng et al., 2025 - Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis
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Fig. 1
Flow chart of gene burden analysis. Exomes of severe adolescent idiopathic scoliosis (AIS) cases and in-house controls went through data cleaning and anchoring to European population. Rare gene burden analyses were performed between 1221 unrelated severe AIS probands with two independent controls (1397 in-house controls and 56885 gnomAD non-Finnish European (NFE) controls) in the autosomal dominant mode using the Testing Rare vAriants using Public Data (TRAPD) method. PCA, principal component analysis. AC, allele count. EA, European American. |
Expression Data
Expression Detail
Antibody Labeling
Phenotype Data
Phenotype Detail
Acknowledgments
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Full text @ J. Med. Genet.