Gene entry
CUL7
cullin 7
- Chromosome
- 6
- Cytoband
- 6p21.1
- Variants (rsID)
- 28
CUL7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.1). Its official name is “cullin 7”. The reference table lists 28 variants (rsID) for this gene.
Clinically classified variants
17 reference-table entries with clinical significance.
- rs139249497Benignsingle nucleotide variant3M syndrome 1
- rs146808129Benignsingle nucleotide variant3M syndrome 1
- rs147056081Benignsingle nucleotide variant3M syndrome 1
- rs147493246Benignsingle nucleotide variant3M syndrome 1
- rs150212051Benignsingle nucleotide variant3M syndrome 1
- rs183119565Benignsingle nucleotide variant3M syndrome 1
- rs34574340Benignsingle nucleotide variant3M syndrome 1
- rs41274912Benignsingle nucleotide variant3M syndrome 1
- rs141692693Conflicting interpretationssingle nucleotide variant3M syndrome 1
- rs144556973Conflicting interpretationssingle nucleotide variant3M syndrome 1
- rs183865568Conflicting interpretationssingle nucleotide variant3M syndrome 1
- rs201135654Conflicting interpretationssingle nucleotide variant3M syndrome 1
- rs552325363Conflicting interpretationssingle nucleotide variant3M syndrome 1
- rs61752334Conflicting interpretationssingle nucleotide variantInborn genetic diseases|3M syndrome 1
- rs121918229Pathogenicsingle nucleotide variant3M syndrome 1|3-M syndrome
- rs201406974Pathogenicsingle nucleotide variant3M syndrome 1
- rs141829168Uncertain significancesingle nucleotide variant3M syndrome 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.