Gene entry
TNC
tenascin C
- Chromosome
- 9
- Cytoband
- 9q33.1
- Variants (rsID)
- 53
TNC is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q33.1). Its official name is “tenascin C”. The reference table lists 53 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs144032672Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 56
- rs2274750Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 56
- rs113301777Not classifiedmissense_variant
- rs17819466Not classifiedsynonymous_variant
Other listed variants
- rs953288
- rs1250028
- rs2236409
- rs3748169
- rs3748170
- rs3827816
- rs4300068
- rs7847271
- rs10982521
- rs11794797
- rs12235159
- rs12237586
- rs12337619
- rs12347433
- rs55643605
- rs61729478
- rs61735551
- rs61736826
- rs61739209
- rs72758642
- rs74810309
- rs75073052
- rs75198247
- rs78520368
- rs114032850
- rs115617492
- rs138416542
- rs139636928
- rs141336913
- rs145797604
- rs146784251
- rs149181557
- rs149285218
- rs149375079
- rs149752009
- rs150508537
- rs151119387
- rs189247379
- rs189493565
- rs199599843
- rs200005353
- rs200193588
- rs200401362
- rs201327197
- rs201357679
- rs201633665
- rs201858433
- rs202234406
- rs377332436
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.