Gene entry
KRT13
keratin 13
- Chromosome
- 17
- Cytoband
- 17q21.2
- Variants (rsID)
- 11
KRT13 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q21.2). Its official name is “keratin 13”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs139318123Benignsingle nucleotide variantWhite sponge nevus 2
- rs142183272Benignsingle nucleotide variantWhite sponge nevus 2
- rs9891361Benignsingle nucleotide variantWhite sponge nevus 2
- rs8182306Not classifiedsynonymous_variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.