Gene entry
CLRN1
clarin 1
- Chromosome
- 3
- Cytoband
- 3q25.1
- Variants (rsID)
- 29
CLRN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q25.1). Its official name is “clarin 1”. The reference table lists 29 variants (rsID) for this gene.
Clinically classified variants
14 reference-table entries with clinical significance.
- rs12635299Benignsingle nucleotide variantUsher syndrome type 3
- rs16846663Benignsingle nucleotide variantUsher syndrome type 3A
- rs6786256Benignsingle nucleotide variant
- rs111033434Conflicting interpretationssingle nucleotide variantRare genetic deafness
- rs121908143Conflicting interpretationssingle nucleotide variantUsher syndrome type 3|Retinal dystrophy|Usher syndrome type 3A
- rs139829306Conflicting interpretationssingle nucleotide variantUsher syndrome type 3
- rs55842922Conflicting interpretationssingle nucleotide variantUsher syndrome type 3
- rs121908141Likely pathogenicsingle nucleotide variantUsher syndrome type 3
- rs111033258Pathogenicsingle nucleotide variantUsher syndrome type 3|Retinitis pigmentosa|Rare genetic deafness|Retinal dystrophy|Usher syndrome type 3A|Retinitis pigmentosa|Usher syndrome type 3A
- rs111033267Pathogenicsingle nucleotide variantUsher syndrome type 3|Retinitis pigmentosa|Rare genetic deafness|Usher syndrome type 3A
- rs121908140Pathogenicsingle nucleotide variantUsher syndrome type 3|Rare genetic deafness|Hearing impairment|Retinitis pigmentosa
- rs374963432Pathogenicsingle nucleotide variantUsher syndrome type 3|Rare genetic deafness|Usher syndrome|Usher syndrome type 3A
- rs397517932PathogenicDeletionUsher syndrome type 3|Rare genetic deafness|Usher syndrome
- rs201008540Uncertain significancesingle nucleotide variantUsher syndrome type 3|Usher syndrome type 3A
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.