Gene entry
USH1G
USH1 protein network component sans
- Chromosome
- 17
- Cytoband
- 17q25.1
- Variants (rsID)
- 7
USH1G is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.1). Its official name is “USH1 protein network component sans”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs111033465Benignsingle nucleotide variantUsher syndrome type 1G
- rs151242039Benignsingle nucleotide variant
- rs147967199Conflicting interpretationssingle nucleotide variant
- rs569032124Conflicting interpretationssingle nucleotide variantUsher syndrome type 1G
- rs201866631Pathogenicsingle nucleotide variantDeafness|Usher syndrome type 1G|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.