Gene entry
TSPEAR
thrombospondin type laminin G domain and EAR repeats
- Chromosome
- 21
- Cytoband
- 21q22.3
- Variants (rsID)
- 65
TSPEAR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.3). Its official name is “thrombospondin type laminin G domain and EAR repeats”. The reference table lists 65 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs140542643Conflicting interpretationssingle nucleotide variant
- rs149481227Conflicting interpretationssingle nucleotide variant
Other listed variants
- rs233232
- rs233272
- rs233276
- rs233279
- rs233299
- rs233314
- rs392451
- rs403603
- rs411254
- rs460380
- rs464504
- rs465360
- rs468278
- rs743492
- rs926195
- rs926196
- rs932281
- rs1004686
- rs1107121
- rs1123949
- rs1296489
- rs2838579
- rs2838589
- rs2838647
- rs2838655
- rs2838659
- rs4818956
- rs7278302
- rs7280667
- rs8126931
- rs8133874
- rs9306108
- rs9974195
- rs9978560
- rs9978932
- rs9984476
- rs12481809
- rs12626853
- rs13051885
- rs61745911
- rs62218855
- rs73233053
- rs73234865
- rs74454903
- rs74906001
- rs75234928
- rs75427465
- rs76514316
- rs77187675
- rs78662628
- rs80102952
- rs116931992
- rs117137417
- rs117185437
- rs117267229
- rs117373347
- rs117630952
- rs117757565
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.