Gene entry
TINF2
TERF1 interacting nuclear factor 2
- Chromosome
- 14
- Cytoband
- 14q12
- Variants (rsID)
- 7
TINF2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q12). Its official name is “TERF1 interacting nuclear factor 2”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs142777869Benignsingle nucleotide variantDyskeratosis congenita, autosomal dominant 1|Dyskeratosis congenita, autosomal dominant 3|Revesz syndrome|Dyskeratosis congenita|Malignant tumor of breast
- rs192423622Conflicting interpretationssingle nucleotide variantDyskeratosis congenita
- rs121918544Pathogenicsingle nucleotide variantDyskeratosis congenita, autosomal dominant 3|Revesz syndrome|Dyskeratosis congenita
- rs121918545Pathogenicsingle nucleotide variantDyskeratosis congenita, autosomal dominant 3|Dyskeratosis congenita, autosomal dominant 1|Dyskeratosis congenita
- rs199422311Not classifiedsingle nucleotide variantDyskeratosis congenita, autosomal dominant 1
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.