Gene entry
GRXCR1
glutaredoxin and cysteine rich domain containing 1
- Chromosome
- 4
- Cytoband
- 4p13
- Variants (rsID)
- 27
GRXCR1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4p13). Its official name is “glutaredoxin and cysteine rich domain containing 1”. The reference table lists 27 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs57655409Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 25
- rs146696590Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 25
- rs267606856Pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 25
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.