Gene entry
INVS
inversin
- Chromosome
- 9
- Cytoband
- 9q31.1
- Variants (rsID)
- 29
INVS is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q31.1). Its official name is “inversin”. The reference table lists 29 variants (rsID) for this gene.
Clinically classified variants
15 reference-table entries with clinical significance.
- rs116222916Benignsingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs116438342Benignsingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs2491097Benignsingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs2787374Benignsingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs41312220Benignsingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs76868679Benignsingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs76975466Benignsingle nucleotide variant
- rs116606949Conflicting interpretationssingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs149315279Conflicting interpretationssingle nucleotide variantNephronophthisis
- rs376879175Conflicting interpretationssingle nucleotide variantNephronophthisis|Infantile nephronophthisis
- rs62577237Likely benignsingle nucleotide variantInfantile nephronophthisis
- rs200844390Pathogenicsingle nucleotide variantInfantile nephronophthisis|Nephronophthisis
- rs150883233Uncertain significancesingle nucleotide variantNephronophthisis
- rs201043963Uncertain significancesingle nucleotide variantNephronophthisis
- rs201904771Uncertain significancesingle nucleotide variantNephronophthisis
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.