Gene entry
GPR179
G protein-coupled receptor 179
- Chromosome
- 17
- Cytoband
- 17q12
- Variants (rsID)
- 30
GPR179 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q12). Its official name is “G protein-coupled receptor 179”. The reference table lists 30 variants (rsID) for this gene.
Clinically classified variants
14 reference-table entries with clinical significance.
- rs111677298Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs148601715Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs149252987Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs150125328Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs201214109Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs59208852Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs72832276Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs74871223Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs79954845Benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs112987826Conflicting interpretationssingle nucleotide variant
- rs147966258Conflicting interpretationssingle nucleotide variantCongenital stationary night blindness 1E
- rs770066665Conflicting interpretationsDeletionCongenital stationary night blindness 1E|Congenital stationary night blindness|Retinal dystrophy
- rs143624972Likely benignsingle nucleotide variantCongenital stationary night blindness 1E
- rs281875236Pathogenicsingle nucleotide variantCongenital stationary night blindness 1E
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.