Gene entry
TSEN2
tRNA splicing endonuclease subunit 2
- Chromosome
- 3
- Cytoband
- 3p25.2
- Variants (rsID)
- 22
TSEN2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p25.2). Its official name is “tRNA splicing endonuclease subunit 2”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs12495784Benignsingle nucleotide variantPontoneocerebellar hypoplasia
- rs142211875Benignsingle nucleotide variantPontoneocerebellar hypoplasia
- rs33955793Benignsingle nucleotide variantPontoneocerebellar hypoplasia
- rs41293385Benignsingle nucleotide variantPontoneocerebellar hypoplasia
- rs62637658Benignsingle nucleotide variant
- rs77899976Benignsingle nucleotide variantPontoneocerebellar hypoplasia
- rs78685815Benignsingle nucleotide variantPontoneocerebellar hypoplasia
- rs113981920Conflicting interpretationssingle nucleotide variantPontoneocerebellar hypoplasia
- rs113994149Conflicting interpretationssingle nucleotide variantPontocerebellar hypoplasia type 2B|Pontoneocerebellar hypoplasia
- rs146117200Conflicting interpretationssingle nucleotide variantPontoneocerebellar hypoplasia
- rs9871742Likely benignsingle nucleotide variantPontoneocerebellar hypoplasia
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.