Gene entry
ROGDI
rogdi atypical leucine zipper
- Chromosome
- 16
- Cytoband
- 16p13.3
- Variants (rsID)
- 11
ROGDI is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “rogdi atypical leucine zipper”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs115660765Benignsingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs138409264Benignsingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs150687774Benignsingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs142481526Conflicting interpretationssingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs148051351Conflicting interpretationssingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs117730440Likely benignsingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs2305659Likely benignsingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs80033521Uncertain significancesingle nucleotide variantAmelocerebrohypohidrotic syndrome
- rs2075465Not classifieddownstream_gene_variant
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.