Gene entry
UNC13D
unc-13 homolog D
- Chromosome
- 17
- Cytoband
- 17q25.1
- Variants (rsID)
- 16
UNC13D is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.1). Its official name is “unc-13 homolog D”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
12 reference-table entries with clinical significance.
- rs112341334Benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3
- rs140758914Benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3
- rs35037984Benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3|Autoinflammatory syndrome
- rs117221419Conflicting interpretationssingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3|Autoinflammatory syndrome
- rs118049905Conflicting interpretationssingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3|Autoinflammatory syndrome
- rs143320460Conflicting interpretationssingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3|Autoinflammatory syndrome
- rs147886860Conflicting interpretationssingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3|Autoinflammatory syndrome
- rs372034111Conflicting interpretationssingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3
- rs147748627Likely benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3
- rs201908137Pathogenicsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3
- rs777759523Pathogenicsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3|Autoinflammatory syndrome
- rs200033170Uncertain significancesingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 3
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.