Gene entry
FLG
filaggrin
- Chromosome
- 1
- Cytoband
- 1q21.3
- Variants (rsID)
- 15
FLG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q21.3). Its official name is “filaggrin”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs146466242Conflicting interpretationssingle nucleotide variantIchthyosis vulgaris
- rs74129447Likely benignsingle nucleotide variant
- rs114733570Pathogenicsingle nucleotide variantIchthyosis vulgaris|FLG-related disorders
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
