Gene entry
UNC13B
unc-13 homolog B
- Chromosome
- 9
- Cytoband
- 9p13.3
- Variants (rsID)
- 37
UNC13B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p13.3). Its official name is “unc-13 homolog B”. The reference table lists 37 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs11790683Not classifiedsynonymous_variant
- rs41315995Not classifiedmissense_variant
Other listed variants
- rs1927962
- rs4419897
- rs4879877
- rs7865406
- rs13293564
- rs28535895
- rs34239190
- rs75735943
- rs75895814
- rs76642371
- rs77002173
- rs78207612
- rs79630819
- rs80133431
- rs80311298
- rs117227802
- rs117619387
- rs118138111
- rs138440338
- rs139333262
- rs139577182
- rs141016510
- rs142442316
- rs146190855
- rs149509924
- rs185611344
- rs190693606
- rs193103550
- rs200053468
- rs200739160
- rs201421861
- rs201901981
- rs202128839
- rs202163094
- rs756677044
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
