Gene entry
GLMN
glomulin, FKBP associated protein
- Chromosome
- 1
- Cytoband
- 1p22.1
- Variants (rsID)
- 20
GLMN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p22.1). Its official name is “glomulin, FKBP associated protein”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs35258161Benignsingle nucleotide variantGlomuvenous malformation
- rs145762716Conflicting interpretationssingle nucleotide variantGlomuvenous malformation|Blue rubber bleb nevus
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.