Gene entry
SLC2A10
solute carrier family 2 member 10
- Chromosome
- 20
- Cytoband
- 20q13.12
- Variants (rsID)
- 23
SLC2A10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20q13.12). Its official name is “solute carrier family 2 member 10”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
18 reference-table entries with clinical significance.
- rs142431229Benignsingle nucleotide variantArterial tortuosity syndrome
- rs201323237Benignsingle nucleotide variantArterial tortuosity syndrome|Cardiovascular phenotype|Familial thoracic aortic aneurysm and aortic dissection
- rs76315093Benignsingle nucleotide variantArterial tortuosity syndrome|Familial thoracic aortic aneurysm and aortic dissection
- rs117587497Conflicting interpretationssingle nucleotide variantArterial tortuosity syndrome|Cardiovascular phenotype|Familial thoracic aortic aneurysm and aortic dissection
- rs121908173Conflicting interpretationssingle nucleotide variantArterial tortuosity syndrome|Cardiovascular phenotype|Familial thoracic aortic aneurysm and aortic dissection
- rs142106322Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Arterial tortuosity syndrome|Familial thoracic aortic aneurysm and aortic dissection
- rs142639587Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Arterial tortuosity syndrome
- rs143301610Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Arterial tortuosity syndrome|Familial thoracic aortic aneurysm and aortic dissection
- rs199848479Conflicting interpretationssingle nucleotide variantArterial tortuosity syndrome|Cardiovascular phenotype
- rs201159437Conflicting interpretationssingle nucleotide variantArterial tortuosity syndrome
- rs34295241Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Arterial tortuosity syndrome|Familial thoracic aortic aneurysm and aortic dissection
- rs377142129Conflicting interpretationssingle nucleotide variantArterial tortuosity syndrome|Familial thoracic aortic aneurysm and aortic dissection
- rs748662135Conflicting interpretationssingle nucleotide variantArterial tortuosity syndrome|Cardiovascular phenotype
- rs771028960Conflicting interpretationssingle nucleotide variantArterial tortuosity syndrome|Cardiovascular phenotype
- rs121908172Pathogenicsingle nucleotide variantArterial tortuosity syndrome
- rs756457861Pathogenicsingle nucleotide variantArterial tortuosity syndrome|Cardiovascular phenotype
- rs139858464Uncertain significancesingle nucleotide variant
- rs199599532Uncertain significancesingle nucleotide variantArterial tortuosity syndrome
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.