Gene entry
TNR
tenascin R
- Chromosome
- 1
- Cytoband
- 1q25.1
- Variants (rsID)
- 132
TNR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q25.1). Its official name is “tenascin R”. The reference table lists 132 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs61731112Conflicting interpretationssingle nucleotide variantParkinson disease
- rs150331590Uncertain significancesingle nucleotide variantParkinson disease
Other listed variants
- rs859357
- rs859363
- rs859371
- rs859374
- rs859400
- rs859413
- rs859433
- rs859438
- rs859455
- rs859460
- rs859471
- rs860905
- rs909741
- rs1103005
- rs1155910
- rs1323123
- rs1351963
- rs1485383
- rs2040425
- rs2171027
- rs2179158
- rs2236883
- rs2239819
- rs2861311
- rs3766680
- rs4233164
- rs4652090
- rs4652099
- rs4652101
- rs4652108
- rs6655978
- rs6659820
- rs6675876
- rs6688098
- rs6691883
- rs7354864
- rs7515041
- rs7515728
- rs7539097
- rs7541077
- rs7544659
- rs9283389
- rs9787193
- rs10798380
- rs10798390
- rs10912985
- rs10913004
- rs10913019
- rs10913043
- rs11579742
- rs11582103
- rs11802001
- rs12024031
- rs12040313
- rs12046065
- rs12065732
- rs12088391
- rs12119177
- rs12144778
- rs12401659
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
