Gene entry

NKX2-1

NK2 homeobox 1

Chromosome: 14
Cytoband: 14q13.3
Variants (rsID): 3

NKX2-1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q13.3). Its official name is “NK2 homeobox 1”. The reference table lists 3 variants (rsID) for this gene.

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Clinically classified variants

2 reference-table entries with clinical significance.

rs137852693Pathogenicsingle nucleotide variantBrain-lung-thyroid syndrome|Inborn genetic diseases|Benign hereditary chorea
rs28936672Pathogenicsingle nucleotide variantBenign hereditary chorea

Other listed variants

rs79781382

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.