Gene entry
UMOD
uromodulin
- Chromosome
- 16
- Cytoband
- 16p12.3
- Variants (rsID)
- 26
UMOD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p12.3). Its official name is “uromodulin”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs13333226Associationsingle nucleotide variantEssential hypertension
- rs13335818Benignsingle nucleotide variantFamilial juvenile hyperuricemic nephropathy type 1
- rs187555378Benignsingle nucleotide variantFamilial juvenile hyperuricemic nephropathy type 1
- rs28544423Benignsingle nucleotide variantFamilial juvenile hyperuricemic nephropathy type 1
- rs55772253Benignsingle nucleotide variantFamilial juvenile hyperuricemic nephropathy type 1
- rs139607138Conflicting interpretationssingle nucleotide variantFamilial juvenile hyperuricemic nephropathy type 1
- rs143583842Conflicting interpretationssingle nucleotide variantFamilial juvenile hyperuricemic nephropathy type 1
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.
