Gene entry
VLDLR
very low density lipoprotein receptor
- Chromosome
- 9
- Cytoband
- 9p24.2
- Variants (rsID)
- 23
VLDLR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p24.2). Its official name is “very low density lipoprotein receptor”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs114172780Benignsingle nucleotide variant
- rs6145Benignsingle nucleotide variantCongenital cerebellar hypoplasia|Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
- rs6149Benignsingle nucleotide variantCongenital cerebellar hypoplasia|Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
- rs116306908Conflicting interpretationssingle nucleotide variant
- rs148487944Conflicting interpretationssingle nucleotide variantCongenital cerebellar hypoplasia|Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
- rs79720897Conflicting interpretationssingle nucleotide variantCongenital cerebellar hypoplasia|Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
- rs35339834Uncertain significancesingle nucleotide variantCongenital cerebellar hypoplasia|Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
- rs35948251Uncertain significancesingle nucleotide variantCongenital cerebellar hypoplasia|Cerebellar ataxia, intellectual disability, and dysequilibrium 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.