Gene entry
MSRB3
methionine sulfoxide reductase B3
- Chromosome
- 12
- Cytoband
- 12q14.3
- Variants (rsID)
- 19
MSRB3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q14.3). Its official name is “methionine sulfoxide reductase B3”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs387907088Pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 74|Hearing loss, autosomal recessive
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.