Gene entry
NFAT5
nuclear factor of activated T cells 5
- Chromosome
- 16
- Cytoband
- 16q22.1
- Variants (rsID)
- 15
NFAT5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q22.1). Its official name is “nuclear factor of activated T cells 5”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs144343499Benignsingle nucleotide variantImmunodeficiency
- rs145602190Benignsingle nucleotide variantImmunodeficiency
- rs56368098Benignsingle nucleotide variantImmunodeficiency
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.
