Gene entry
MT-RNR1
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 23
MT-RNR1 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
23 reference-table entries with clinical significance.
- rs111033179Benignsingle nucleotide variant
- rs111033213Benignsingle nucleotide variant
- rs111033322Benignsingle nucleotide variant
- rs111033358Benignsingle nucleotide variant
- rs2000974Benignsingle nucleotide variant
- rs2001030Benignsingle nucleotide variant
- rs28358572Benignsingle nucleotide variant
- rs28358573Benignsingle nucleotide variant
- rs2856982Benignsingle nucleotide variant
- rs727503164Benignsingle nucleotide variant
- rs28358569Drug responsesingle nucleotide variantMitochondrial non-syndromic sensorineural hearing loss|Aminoglycoside-induced deafness|Gentamicin response
- rs111033354Likely benignsingle nucleotide variant
- rs200887992Likely benignsingle nucleotide variant
- rs267606620Likely benignsingle nucleotide variantMitochondrial non-syndromic sensorineural hearing loss
- rs386828880Likely benignsingle nucleotide variant
- rs386828884Likely benignsingle nucleotide variant
- rs3888511Likely benignsingle nucleotide variantMitochondrial non-syndromic sensorineural hearing loss
- rs397515731Likely benignsingle nucleotide variant
- rs58327546Likely benignsingle nucleotide variant
- rs727503163Likely benignsingle nucleotide variant
- rs727503165Likely benignsingle nucleotide variant
- rs397515729Uncertain significancesingle nucleotide variant
- rs2853518Not classifiedsingle nucleotide variant
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.