Gene entry
RHAG
Rh associated glycoprotein
- Chromosome
- 6
- Cytoband
- 6p12.3
- Variants (rsID)
- 25
RHAG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p12.3). Its official name is “Rh associated glycoprotein”. The reference table lists 25 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs16879498Benignsingle nucleotide variantRh-null, regulator type
- rs104893987Othersingle nucleotide variant
- rs121918586Pathogenicsingle nucleotide variantRh mod blood group phenotype
- rs375508949Pathogenicsingle nucleotide variantRh-null, regulator type
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.
