Gene entry
GRHPR
glyoxylate and hydroxypyruvate reductase
- Chromosome
- 9
- Cytoband
- 9p13.2
- Variants (rsID)
- 17
GRHPR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p13.2). Its official name is “glyoxylate and hydroxypyruvate reductase”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs200106110Benignsingle nucleotide variantPrimary hyperoxaluria, type II
- rs2736664Benignsingle nucleotide variantPrimary hyperoxaluria, type II
- rs309458Benignsingle nucleotide variantPrimary hyperoxaluria, type II
- rs41303225Benignsingle nucleotide variantPrimary hyperoxaluria, type II
- rs56401536Benignsingle nucleotide variantPrimary hyperoxaluria, type II
- rs78920863Conflicting interpretationssingle nucleotide variantPrimary hyperoxaluria, type II
- rs180177307Likely pathogenicsingle nucleotide variantPrimary hyperoxaluria, type II
- rs180177317Likely pathogenicsingle nucleotide variantPrimary hyperoxaluria, type II
- rs180177320OtherDeletion
- rs180177316PathogenicDeletionPrimary hyperoxaluria, type II
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.