Gene entry
KAT6B
lysine acetyltransferase 6B
- Chromosome
- 10
- Cytoband
- 10q22.2
- Variants (rsID)
- 35
KAT6B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q22.2). Its official name is “lysine acetyltransferase 6B”. The reference table lists 35 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs182392778Benignsingle nucleotide variantGenitopatellar syndrome
- rs3740321Benignsingle nucleotide variantGenitopatellar syndrome
- rs140989004Uncertain significancesingle nucleotide variantGenitopatellar syndrome
- rs140992439Uncertain significancesingle nucleotide variantGenitopatellar syndrome
Other listed variants
- rs951308
- rs1551067
- rs1551068
- rs4307657
- rs7075439
- rs7899137
- rs7917746
- rs10466033
- rs10490991
- rs12221048
- rs12571012
- rs16931793
- rs17641765
- rs41280426
- rs41304619
- rs58499280
- rs60517985
- rs72803443
- rs76368925
- rs78786092
- rs80105154
- rs117595313
- rs117901502
- rs138617006
- rs143733161
- rs144278945
- rs189002123
- rs192187772
- rs200728982
- rs201828896
- rs202037961
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.