Gene entry
DSG4
desmoglein 4
- Chromosome
- 18
- Cytoband
- 18q12.1
- Variants (rsID)
- 24
DSG4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18q12.1). Its official name is “desmoglein 4”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs16959856Benignsingle nucleotide variantHypotrichosis 6
- rs34620697Benignsingle nucleotide variantHypotrichosis 6
- rs36101975Benignsingle nucleotide variantHypotrichosis 6
- rs150676638Conflicting interpretationssingle nucleotide variantHypotrichosis 6
- rs35378785Conflicting interpretationssingle nucleotide variantHypotrichosis 6
- rs117510013Likely benignsingle nucleotide variantHypotrichosis 6
- rs267606775Pathogenicsingle nucleotide variantHypotrichosis 6
- rs267606776Pathogenicsingle nucleotide variantHypotrichosis 6
- rs147705128Uncertain significancesingle nucleotide variantHypotrichosis 6
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.